KR20210144593A - Salt, acid generator, resist composition and method for producing resist pattern - Google Patents

Abstract

The objective of the present invention is to prepare a resist pattern with good critical dimension uniformity (CDU). To this end, the present invention provides a salt represented by chemical formula (I), and an acid generator and resist composition comprising the same. In the chemical formula; R^1 and R^2 represent a hydroxyl group, -O-L^1-CO-O-R^10, and the like, independently and respectively; L^1 represents an alkanediyl group; R^4, R^5, R^7 and R^8 represent a halogen atom, a fluorinated alkyl group or a hydrocarbon group, independently and respectively, wherein the hydrocarbon group may have a substituent, and -CH_2- contained in the hydrocarbon group may be substituted with -O- or -CO-, and the like; R^10 represents an acid labile group; X^1 and X^2 represent an oxygen atom or a sulfur atom, independently and respectively; m^1 represents an integer from 1 to 5, m^2 and m^8 represent an integer from 0 to 5, and m^4, m^5 and m^7 represent an integer from 0 to 4; and AI^- represents an organic anion.

Description

Salt, acid generator, resist composition, and method for producing a resist pattern {SALT, ACID GENERATOR, RESIST COMPOSITION AND METHOD FOR PRODUCING RESIST PATTERN}

[0001] The present invention relates to a salt, an acid generator, a resist composition, and a method for producing a resist pattern.

[0002] Patent Document 1 describes a resist composition containing a salt represented by the following formula as an acid generator.

Non-patent document 1 describes a salt represented by the following formula.

[0003] Patent Document 2 describes a salt represented by the following formula.

Patent Document 3 describes a salt represented by the following formula.

Patent Document 4 describes a salt represented by the following formula.

[0004] 1. Japanese Patent Laid-Open No. 2011-006400 2. Japanese Patent Laid-Open No. 2017-155036 3. Japanese Patent Laid-Open No. H06-118651 4. Japanese Patent Laid-Open No. H08-160620

[0005] 1. Org. Lett. 2018, 20, 4458-4461

[0006] An object of the present invention is to provide a salt that forms a resist pattern having better CD uniformity (Critical Dimension uniformity) than a resist pattern formed from a resist composition containing the salt. do.

[0007] The present invention includes the following inventions.

[1] A salt represented by formula (I).

[In formula (I),

R ¹ and R ² each independently represent a hydroxyl group, -OR ¹⁰ , -O-CO-OR ¹⁰ , or -OL ¹ -CO-OR ¹⁰ .

L ¹ represents an alkanediyl group having 1 to 6 carbon atoms.

R ⁴ , R ⁵ , R ⁷ and R ⁸ each independently represent a halogen atom, a fluorinated alkyl group having 1 to 12 carbon atoms or a hydrocarbon group having 1 to 18 carbon atoms, the hydrocarbon group may have a substituent, and the hydrocarbon group -CH ₂ - contained may be substituted with -O-, -CO-, -S-, or -SO _{2 -.}

R ¹⁰ represents an acid labile group.

X ¹ and X ² each independently represent an oxygen atom or a sulfur atom.

m1 represents the integer in any one of 1-5, and when m1 is 2 or more, the group in some parenthesis may mutually be same or different.

m2 represents the integer in any one of 0-5, and when m2 is 2 or more, the group in some parenthesis may mutually be same or different.

m4 represents the integer in any one of 0-4, and when m4 is 2 or more, some R<^4> may mutually be same or different.

m5 represents the integer in any one of 0-4, and when m5 is 2 or more, some R<^5> may mutually be same or different.

m7 represents the integer in any one of 0-4, and when m7 is 2 or more, some R<^7> may mutually be same or different.

m8 represents the integer in any one of 0-5, and when m8 is 2 or more, some R<^8> may mutually be same or different.

However, 1≤m1+m7≤5 and 0≤m2+m8≤5.

AI ^- represents an organic anion.]

[2] The salt according to [1], wherein ^{X 1} and X ^{2 are oxygen atoms.}

[3] The ^{salt according to [1] or [2], wherein the acid labile group of R 10} is a group represented by the formula (1a) or a group represented by the formula (2a).

Equation (1a) of, R ^aa1, R ^aa2 and R ^aa3 is, may each independently have an alkyl group having 1 to 8 carbon atoms which may have a substituent, an alkenyl group having a carbon number of 2-8 that may have a substituent the substituents represents an alicyclic hydrocarbon group having 3 to 20 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent, or R ^aa1 and R ^aa2 are bonded to each other and together with the carbon atom to which they are bonded, have 3 to 20 carbon atoms Forms an alicyclic hydrocarbon group.

* indicates a bonding hand.]

[In formula (2a), R ^aa1' and R ^aa2' each independently represent a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, and R ^aa3' represents a hydrocarbon group having 1 to 20 carbon atoms, or R ^{aa2 '} and R ^aa3' combine with each other to form a heterocyclic group having 3 to 20 carbon atoms together with ^{-CX a} - to which they are bonded _{, and -CH 2} - included in the hydrocarbon group and the heterocyclic group is -O- or - It may be substituted with S-.

X ^a represents an oxygen atom or a sulfur atom.

* indicates a bonding hand.]

[4] The salt according to any one of [1] to [3], ^{wherein R 1} and R ² each independently represent a hydroxyl group, OR ¹⁰ , or -OL ¹ -CO-OR ^{10 .}

[5] The salt according to any one of [1] to [4], wherein m2 is 0, m8 is 1, and R ^{8 is a branched alkyl group having 3 or 4 carbon atoms.}

[6] The salt according to any one of [1] to [5], wherein the bonding position of ^{R 1 is bonded at the p position with respect to the bonding position of X 1 .}

[7] AI ^- salt according to the, sulfonic acid anion, any of the sulfonyl imide anion, a sulfonate anion or carboxylic acid anion suited nilme [1] to [6].

[8] The ^{salt according to any one of [1] to [7], wherein AI −} is a sulfonic acid anion, and the sulfonic acid anion is an anion represented by formula (IA).

[In formula (I-A),

Q ¹ and Q ² each independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.

L ¹ represents a saturated hydrocarbon group having 1 to 24 carbon atoms, -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O- or -CO-, and a hydrogen atom contained in the saturated hydrocarbon group is fluorine It may be substituted with an atom or a hydroxyl group.

Y ¹ represents a methyl group which may have a substituent or an alicyclic hydrocarbon group having 3 to 24 carbon atoms which may have a substituent, and -CH ₂ - contained in the alicyclic hydrocarbon group is -O-, -SO ₂ - or - It may be substituted with CO-.]

[9] An acid generator containing the salt according to any one of [1] to [8].

[10] A resist composition comprising the acid generator according to [9] and a resin having an acid labile group.

[11] [10] wherein the resin having an acid-labile group contains at least one selected from the group consisting of a structural unit represented by formula (a1-1) and a structural unit represented by formula (a1-2). The resist composition according to ].

[In formulas (a1-1) and (a1-2),

L ^a1 and L ^a2 each independently represent -O- or *-O-(CH ₂ ) _k1 -CO-O-, k1 represents an integer of any one of 1 to 7, and * is -CO- represents a bond with

R ^a4 and R ^a5 each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.

R ^a6 and R ^a7 each independently represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a group combining them. .

m1 represents the integer in any one of 0-14.

n1 represents the integer in any one of 0-10.

n1' represents the integer in any one of 0-3.]

[12] The resist composition according to [10] or [11], wherein the resin having an acid labile group includes a structural unit represented by formula (a2-A).

[In formula (a2-A),

R ^a50 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.

R ^a51 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an alkoxyalkyl group having 2 to 12 carbon atoms, an alkoxyalkoxy group having 2 to 12 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms, and an alkylcarbonyl group having 2 to 4 carbon atoms. An alkylcarbonyloxy group, acryloyloxy group or methacryloyloxy group which is 2-4 is represented.

A ^a50 represents a single bond or ^* -X ^a51 -(A ^a52 -X ^a52 ) _nb -, and * represents a bond with the carbon atom to which ^{-R a50 is bonded.}

A ^a52 represents a C1-C6 alkanediyl group.

X ^a51 and X ^a52 each independently represent -O-, -CO-O- or -O-CO-.

nb represents 0 or 1.

mb represents any integer from 0 to 4. When mb is any integer of 2 or more, a plurality of R ^a51 may be the same or different from each other.]

[13] The resist composition according to any one of [10] to [12], further comprising a salt that generates an acid having a weaker acidity than the acid generated from the acid generator.

[14] (1) a step of applying the resist composition according to any one of [10] to [13] on a substrate;

(2) drying the composition after application to form a composition layer;

(3) a step of exposing the composition layer;

(4) heating the composition layer after exposure, and

(5) The manufacturing method of a resist pattern including the process of developing the composition layer after heating.

[0008] By using the resist composition containing the salt of the present invention, it is possible to produce a resist pattern with good CD uniformity (CDU).

[0009] In the present specification, "(meth)acrylic monomer" means "at least one type of an acrylic monomer and a methacrylic monomer". Notations, such as "(meth)acrylate" and "(meth)acrylic acid", also show the same meaning. The group described in this specification WHEREIN: About the thing which can take both a linear structure and a branched structure, any may be sufficient. _{When -CH 2} - contained in a hydrocarbon group or the like is substituted with -O-, -S-, -CO- or -SO ₂ -, the same example applies to each group. "Combined group" means the group which couple|bonded 2 or more types of the illustrated groups, You may change suitably the valence of these groups according to the bonding form. "Derived" or "derived" indicates that the polymerizable C=C bond contained in the molecule becomes a -CC- group by polymerization. When stereoisomers exist, all stereoisomers are included.

[Salt Represented by Formula (I)]

The present invention relates to a salt represented by formula (I) (hereinafter sometimes referred to as “salt (I)”).

Among salts (I), the side having a negative charge is sometimes called "anion (I)", and the side having a positive charge is called "cation (I)" in some cases.

[In the formula, all the symbols each have the same meaning as above.]

[0011] In Formula (I), as the alkanediyl group in L ^{1 included in R 1} and R ² , a methylene group, ethylene group, propane-1,3-diyl group, butane-1,4-diyl group linear alkanediyl groups such as diyl, pentane-1,5-diyl group and hexane-1,6-diyl group; and

Ethane-1,1-diyl group, propane-1,1-diyl group, propane-1,2-diyl group, propane-2,2-diyl group, pentane-2,4-diyl group, 2-methylpropane- and branched alkanediyl groups such as 1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group, and 2-methylbutane-1,4-diyl group. .

It is preferable that it is a C1-C3 alkanediyl group, and, as for L<^{1>, it is more preferable that it is a methylene group.}

[0012] ^{The acid labile group of R 10} included in ^{R 1} and R ² means a group that forms a carboxy group or a hydroxy group by leaving the group represented by ^{R 10} when it comes into contact with an acid (eg, trifluoromethanesulfonic acid).

Examples of the acid-labile group include a group represented by the formula (1a) (hereinafter sometimes referred to as “acid-labile group (1a)”), a group represented by the formula (2a) (hereinafter sometimes referred to as “acid-labile group”). (2a)") is preferable.

Equation (1a) of, R ^aa1, R ^aa2 and R ^aa3 is, may each independently have an alkyl group having 1 to 8 carbon atoms which may have a substituent, an alkenyl group having a carbon number of 2-8 that may have a substituent the substituents represents an alicyclic hydrocarbon group having 3 to 20 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent, or R ^aa1 and R ^aa2 are bonded to each other and together with the carbon atom to which they are bonded, have 3 to 20 carbon atoms Forms an alicyclic hydrocarbon group.

* indicates a bonding hand.]

[In formula (2a), R ^aa1' and R ^aa2' each independently represent a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, and R ^aa3' represents a hydrocarbon group having 1 to 20 carbon atoms, or R ^{aa2 '} and R ^aa3' combine with each other to form a heterocyclic group having 3 to 20 carbon atoms together with ^{-CX a} - to which they are bonded _{, and -CH 2} - included in the hydrocarbon group and the heterocyclic group is -O- or - It may be substituted with S-.

X ^a represents an oxygen atom or a sulfur atom.

* indicates a bonding hand.]

[0013] R ^{aa1, aa2} R and R alkyl group of ^aa3, methyl, ethyl, propyl, n- butyl, n- pentyl, n- hexyl, n- heptyl, n- octyl group, etc. include have. R ^{aa1, aa2} carbon number of the alkyl group of R and R ^aa3 is preferably 1-6, more preferably 1-3.

As the alkenyl group of R ^{aa1, aa2} R and R ^aa3, ethene group, propene group, iso-propene group, butene group, isobutene group, tert- butene group, a pentene group, a hexene group, a heptene group, oktin group, iso Octynyl group and nonenyl group are mentioned.

R ^{aa1, aa2} group is an alicyclic hydrocarbon group of R and R ^aa3, is even and is any one of a monocyclic cyclic. Examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group and a cyclooctyl group. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a norbornyl group, and the following groups (* represents a bond). R ^aa1, the carbon number of the alicyclic hydrocarbon group of R ^aa2 and ^aa3 R is preferably 3-16, more preferably 3-12.

R ^{aa1, aa2,} and R as the aromatic hydrocarbon group of R ^aa3, there may be mentioned a phenyl group, a naphthyl group, an anthryl group, a biphenyl group, an aryl group such as a phenanthryl group. R ^aa1, the number of carbon atoms of the aromatic hydrocarbon group of R ^aa2 and ^aa3 R is preferably 6-14, more preferably 6-10.

Examples of the substituent of the alkyl group having 1 to 8 carbon atoms which may have a substituent include an alkenyl group having 2 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 20 carbon atoms, and an aromatic hydrocarbon group having 6 to 18 carbon atoms. As a substituent of the C2-C8 alkenyl group which may have a substituent, a C1-C8 alkyl group, a C3-C20 alicyclic hydrocarbon group, and a C6-C18 aromatic hydrocarbon group are mentioned. As a substituent of the C3-C20 alicyclic hydrocarbon group which may have a substituent, a C1-C8 alkyl group, a C2-C8 alkenyl group, and a C6-C18 aromatic hydrocarbon group are mentioned. Examples of the substituent of the aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent include an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, and an alicyclic hydrocarbon group having 3 to 20 carbon atoms. More specifically, a group combining the above-mentioned alkyl group and alicyclic hydrocarbon group (eg, methylcyclohexyl group, dimethylcyclohexyl group, methylnorbornyl group, cyclohexylmethyl group, adamantylmethyl group, adamantyldimethyl group, norbornyl group) Alkylcycloalkyl group or cycloalkylalkyl group such as ethyl group), aralkyl group such as benzyl group, aromatic hydrocarbon group having an alkyl group (p-methylphenyl group, p-tert-butylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group) , 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), aromatic hydrocarbon group having an alicyclic hydrocarbon group (p-cyclohexylphenyl group, p-adamantylphenyl group, etc.), phenylcyclohexyl group, etc. an aryl-cycloalkyl group; and the like.

[0015] may be bonded to each other is R R ^aa1 and ^aa2 as ^{-C (R aa1) (R aa2} ) (R aa3) in the case of forming an alicyclic hydrocarbon group together with the carbon atom, a group of the. An alicyclic hydrocarbon group becomes like this. Preferably it is 3-16, More preferably, it is C3-C12. * represents a bond with -O-.

[0016] formula (1a) as the groups represented by, 1,1,1-tree group (formula (1a) in the R ^{aa1, aa2} R and R is an alkyl group of ^aa3 group, preferably a tert- butoxycarbonyl group) ^{, 2-alkyladamantan} -2-yl group (in formula (1a), R ^aa1 , R ^aa2 and the carbon atom to which they are bonded form an adamantyl group, and R aa3 is an alkyl group) and 1-(adamantane) of 1-yl) -1,1-di-alkyl (formula (1a), R and R ^aa1 and ^aa2 is an alkyl group, R ^aa3 is ah, and the like due adamantyl group).

[0017] ^{Examples of the hydrocarbon group of R aa1'} , R ^aa2' and R ^aa3' include an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group formed by combining these groups.

Alkyl group and the alicyclic hydrocarbon group, a group illustrated as R ^{aa1, aa2} R and R ^aa3 are the same.

As an aromatic hydrocarbon group, aryl groups, such as a phenyl group, a naphthyl group, an anthryl group, a biphenyl group, and a phenanthryl group, etc. are mentioned.

As a combined group, the group which combined the above-mentioned alkyl group and alicyclic hydrocarbon group (for example, methylcyclohexyl group, dimethylcyclohexyl group, methylnorbornyl group, cyclohexylmethyl group, adamantylmethyl group, adamantyldimethyl group, norbornyl group) A cycloalkylalkyl group or alkylcycloalkyl group such as an ethyl group), an aralkyl group such as a benzyl group, or an aromatic hydrocarbon group having an alkyl group (p-methylphenyl group, p-tert-butylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group) , 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), aromatic hydrocarbon group having an alicyclic hydrocarbon group (p-cyclohexylphenyl group, p-adamantylphenyl group, etc.), phenylcyclohexyl group, etc. An aryl-cycloalkyl group etc. are mentioned.

^Aa2 R ^'and R ^aa3' a case of forming a heterocyclic group together with the carbon atom and X ^a which they are attached are bonded to each ^{other, -C (R aa1 ') (} R aa2') -X a - (R aa3 ') as the , the following groups are mentioned. * represents a bond.

It is preferable that at least one of R ^aa1' and R ^{aa2' is a hydrogen atom.}

Specific examples of the acid labile group (1a) include the following groups. * indicates a bond.

Specific examples of the acid labile group (2a) include the following groups. * indicates a bond.

The bonding position of R ¹ and R ² may be any of the o position, the m position, and the p position with respect to the bonding position of ^{X 1} and X ^{2 , respectively.} Among these, it is preferable to couple|bond with the p-position with respect to the bonding position of ^X<1> and X<^2>.

R ¹ and R ² are each independently preferably a hydroxyl group, -OR ¹⁰ or -OL ¹ -CO-OR ¹⁰ , each independently more preferably -OR ¹⁰ or -OL ¹ -CO-OR ¹⁰ do.

[0020] Examples ^{of the halogen atom of R 4} , R ⁵ , R ⁷ and R ⁸ include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

The ^{fluorinated alkyl group having 1 to 6 carbon atoms in R 4} , R ⁵ , R ⁷ and R ⁸ represents an alkyl group having 1 to 6 carbon atoms having a fluorine atom, and a perfluoroalkyl group having 1 to 6 carbon atoms (trifluoromethyl group, penta fluoroethyl group, heptafluoropropyl group, nonafluorobutyl group), and 2,2,2-trifluoroethyl group, 3,3,3-trifluoropropyl group, 4,4,4-trifluoro butyl group and 3,3,4,4,4-pentafluorobutyl group. Carbon number of a fluorinated alkyl group becomes like this. Preferably it is 1-4, More preferably, it is 1-3.

Examples of the hydrocarbon group having 1 to 18 carbon atoms for R ⁴ , R ⁵ , R ⁷ and R ⁸ include a chain hydrocarbon group such as an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group formed by combining these groups.

Examples of the alkyl group include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, pentyl group, hexyl group, heptyl group, 2-ethylhexyl group, octyl group, no A nyl group, a decyl group, an undecyl group, a dodecyl group, etc. are mentioned. Carbon number of an alkyl group becomes like this. Preferably it is 1-12, More preferably, it is 1-9, More preferably, it is 1-6, More preferably, it is 1-4.

As an alicyclic hydrocarbon group, either monocyclic or polycyclic may be sufficient, and the group etc. which are shown below are mentioned. The binding site may be in any position.

Specific examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as cyclopropyl group, cyclobutyl group, cyclopentyl group, cyclohexyl group, cycloheptyl group, cyclooctyl group and cyclodecyl group. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, and a norbornyl group. Carbon number of an alicyclic hydrocarbon group becomes like this. Preferably it is 3-18, More preferably, it is 3-16, More preferably, it is 3-12.

A phenyl group, a naphthyl group, a biphenyl group, an anthryl group, a phenanthryl group, a binaphthyl group etc. are mentioned as an aromatic hydrocarbon group. Carbon number of an aromatic hydrocarbon group becomes like this. Preferably it is 6-18, More preferably, it is 6-14, More preferably, it is 6-10.

[0021] As a group formed by combining an aromatic hydrocarbon group and a chain hydrocarbon group (e.g., aromatic hydrocarbon group-alkanediyl group-*, alkyl group-aromatic hydrocarbon group-*, the alkanediyl group and the alkyl group included in the group) -CH ₂ - may be substituted with -O-, -CO-, -S- or -SO ₂ -), a group combining an alicyclic hydrocarbon group and a chain hydrocarbon group (eg, an alicyclic hydrocarbon group-alkanedi group) Diyl-*, alkyl group-alicyclic hydrocarbon group-*, -CH ₂ - contained in the alkanediyl group and the alkyl group may be substituted with -O-, -CO-, -S- or -SO _{2 -.)} , a group in which an aromatic hydrocarbon group and an alicyclic hydrocarbon group are combined (eg, aromatic hydrocarbon group-alicyclic hydrocarbon group-*, alicyclic hydrocarbon group-aromatic hydrocarbon group-*). * indicates a binding site.

As aromatic hydrocarbon group - alkanediyl group -*, aralkyl groups, such as a benzyl group and a phenethyl group, are mentioned.

Examples of the alkyl group-aromatic hydrocarbon group-* include a tolyl group, a xylyl group, and a cumenyl group.

Examples of the alicyclic hydrocarbon group-alkanediyl group-* include cyclohexylmethyl group, cyclohexylethyl group, 1-(adamantan-1-yl)methyl group, 1-(adamantan-1-yl)-1-methylethyl group, etc. and a cycloalkylalkyl group of

Examples of the alkyl group-alicyclic hydrocarbon group-* include a cycloalkyl group having an alkyl group such as a methylcyclohexyl group, a dimethylcyclohexyl group, and a 2-alkyladamantan-2-yl group.

Examples of the aromatic hydrocarbon group-alicyclic hydrocarbon group-* include a phenylcyclohexyl group and the like.

Examples of the alicyclic hydrocarbon group-aromatic hydrocarbon group-* include a cyclohexylphenyl group.

In addition, in a combination, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a chain hydrocarbon group may combine 2 or more types, respectively. Moreover, any group may couple|bond with the benzene ring.

[0022] As a group in which -CH ₂ - contained in the hydrocarbon group is substituted with -O-, -CO-, -S- or -SO ₂ -, a hydroxy group (-CH ₂ - contained in a methyl group, -O- a group substituted with), a carboxy group (a group substituted with -CH ₂ -CH ₂ -valent in an ethyl group, -O-CO-), an alkoxy group (a -CH ₂ -valent at any position included in an alkyl group, - group substituted with O-), thiol (group substituted with -CH _{2 -valent in the methyl group, -S-), alkoxycarbonyl group (-CH 2} -CH ₂ -valent at any position included in the alkyl group, - A group substituted with O-CO-), an alkylcarbonyl group (a group in which -CH ₂ - at any position included in the alkyl group is substituted with -CO-), an alkylthio group (-CH at any position included in the alkyl group) ₂ -valent, a group substituted with -S-), an alkylsulfonyl group (a group substituted with -CH ₂ - at any position included in the alkyl, -SO ₂ -), an alkylcarbonyloxy group (contained in the alkyl group) _{-CH 2} -CH ₂ - at any position being a group substituted with -CO-O-), a cycloalkoxy group, a cycloalkylalkoxy group, an alkoxycarbonyloxy group, an aromatic hydrocarbon group-carbonyloxy group, these The group etc. which combined 2 or more types among groups are mentioned.

Examples of the alkoxy group include an alkoxy group having 1 to 17 carbon atoms, for example, a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentyloxy group, a hexyloxy group, an octyloxy group, a 2-ethylhexyloxy group, a no A nyloxy group, a decyloxy group, an undecyloxy group, etc. are mentioned. Carbon number of an alkoxy group becomes like this. Preferably it is 1-11, More preferably, it is 1-6, More preferably, it is 1-4.

As an alkylthio group, a C1-C12 alkylthio group is mentioned, For example, a methylthio group, an ethylthio group, a propylthio group, a butylthio group, etc. are mentioned. Carbon number of an alkylthio group becomes like this. Preferably it is 1-6, More preferably, it is 1-4.

Examples of the alkylsulfonyl group include an alkylsulfonyl group having 1 to 12 carbon atoms, and examples thereof include a methylsulfonyl group, an ethylsulfonyl group, and a propylsulfonyl group. Carbon number of an alkylsulfonyl group becomes like this. Preferably it is 1-11, More preferably, it is 1-6, More preferably, it is 1-4.

The alkoxycarbonyl group, the alkylcarbonyl group, and the alkylcarbonyloxy group represent groups in which a carbonyl group or a carbonyloxy group is bonded to the above-described alkyl group or alkoxy group.

As an alkoxycarbonyl group, a C2-C17 alkoxycarbonyl group is mentioned, For example, a methoxycarbonyl group, an ethoxycarbonyl group, a butoxycarbonyl group, etc. are mentioned. As an alkylcarbonyl group, a C2-C18 alkylcarbonyl group is mentioned, For example, an acetyl group, a propionyl group, a butyryl group, etc. are mentioned. As an alkylcarbonyloxy group, a C2-C17 alkylcarbonyloxy group is mentioned, For example, an acetyloxy group, a propionyloxy group, a butyryloxy group, etc. are mentioned. Carbon number of an alkoxycarbonyl group becomes like this. Preferably it is 2-11, More preferably, it is 2-6, More preferably, it is 2-4. Carbon number of an alkylcarbonyl group becomes like this. Preferably it is 2-12, More preferably, it is 2-6, More preferably, it is 2-4. Carbon number of an alkylcarbonyloxy group becomes like this. Preferably it is 2-11, More preferably, it is 2-6, More preferably, it is 2-4.

As a cycloalkoxy group, a C3-C17 cycloalkoxy group is mentioned, For example, a cyclohexyloxy group etc. are mentioned. As a cycloalkyl alkoxy group, a C4-C17 cycloalkyl alkoxy group is mentioned, For example, a cyclohexyl methoxy group etc. are mentioned. As an alkoxycarbonyloxy group, a C2-C16 alkoxycarbonyloxy group is mentioned, For example, a butoxycarbonyloxy group etc. are mentioned. Examples of the aromatic hydrocarbon group-carbonyloxy group include an aromatic hydrocarbon group-carbonyloxy group having 7 to 17 carbon atoms, and examples thereof include a benzoyloxy group.

_{[0023] Examples of the group in which -CH 2} - contained in the alicyclic hydrocarbon group is substituted with -O-, -CO-, -S- or -SO ₂ - include groups shown below. The binding site may be in any position. In the groups shown below, the position of -O- may be substituted with _{-S-, and the position of -CO- may be substituted with -SO 2 -, respectively.}

_{When -CH 2} - contained in the hydrocarbon group is substituted with -O- or -CO-, the number of carbon atoms before substitution is the total number of carbon atoms in the hydrocarbon group. In addition, the number may be one, and two or more may be sufficient as it.

[0024] ^{Examples of the substituent which the hydrocarbon group of R 4} , R ⁵ , R ⁷ and R ⁸ may have include a halogen atom, a cyano group, and an alkyl group having 1 to 12 carbon atoms (-CH ₂ - contained in the alkyl group is -O- or -CO- may be substituted).

As a halogen atom, the group similar to the group mentioned above is mentioned.

Examples of the alkyl group having 1 to 12 carbon atoms include the same groups as those described above.

As a substituent, when -CH ₂ - contained in the alkyl group is substituted with -O- or -CO-, the number of carbon atoms before substitution is the total number of carbon atoms in the alkyl group. Examples of the substituted group include a hydroxyl group (a group in which -CH ₂ - contained in a methyl group is substituted with -O-), a carboxy group (a group in which -CH ₂ -CH ₂ - contained in an ethyl group is substituted with -O-CO-) ), an alkoxy group (a group in which -CH ₂ - at any position included in the alkyl group is substituted with -O-), an alkoxycarbonyl group (-CH ₂ -CH ₂ - at any position included in the alkyl group, -O _{A group substituted with -CO-), an alkylcarbonyl group (a group in which -CH 2} - at any position included in the alkyl group is substituted with -CO-), an alkylcarbonyloxy group (at any position included in the alkyl group - group in which CH ₂ -CH ₂ - is substituted with -CO-O-) and the like.

The alkoxy group, alkoxycarbonyl group, alkylcarbonyl group and alkylcarbonyloxy group include, for example, an alkoxy group having 1 to 11 carbon atoms, an alkoxycarbonyl group having 2 to 11 carbon atoms, an alkylcarbonyl group having 2 to 12 carbon atoms, and an alkylcarbonyloxy group having 2 to 11 carbon atoms. group, and the same group as the above-mentioned group can be mentioned.

The hydrocarbon group may have one substituent or a plurality of substituents.

[0025] X ¹ is preferably an oxygen atom.

X ² is preferably oxygen atom.

The bonding position of X ¹ and X ² may be any of the o position, the m position, and the p position with respect to the bonding position of ^{I + .} Among these, it is preferable to couple|bond with the m-position or p-position with respect to the bonding position of ^{I +, and it is more preferable to couple|bond with the p-position.}

It is preferable that it is 1 or 2, and, as for m1, it is more preferable that it is 1.

It is preferable that m2 is 0, 1 or 2.

It is preferable that it is 0, 1, 2, or 4, and, as for m4, it is more preferable that it is 0.

It is preferable that m5 is 0 or 1.

It is preferable that it is 0, 1 or 2, and, as for m7, it is more preferable that it is 0 or 1.

It is preferable that m8 is 0 or 1.

R ⁴ and R ⁵ are each independently a halogen atom, a fluorinated alkyl group having 1 to 4 carbon atoms, or an alkyl group having 1 to 6 carbon atoms (-CH ₂ - contained in the alkyl group is substituted with -O- or -CO-, may be present.), preferably a halogen atom, a fluorinated alkyl group having 1 to 4 carbon atoms, or an alkyl group having 1 to 4 carbon atoms (-CH ₂ - contained in the alkyl group may be substituted with -O- or -CO- .) is more preferable, and it is still more preferable that they are a fluorine atom, an iodine atom, a trifluoromethyl group, or a C1-C4 alkyl group.

R ⁷ and R ⁸ are each independently a halogen atom, a fluorinated alkyl group having 1 to 4 carbon atoms, or an alkyl group having 1 to 6 carbon atoms (-CH ₂ - included in the alkyl group is substituted with -O- or -CO-, may be present.), preferably a halogen atom, a fluorinated alkyl group having 1 to 4 carbon atoms, or an alkyl group having 1 to 4 carbon atoms (-CH ₂ - contained in the alkyl group may be substituted with -O- or -CO- .) is more preferable, and a fluorine atom, an iodine atom, a perfluoroalkyl group having 1 to 4 carbon atoms, or an alkyl group having 1 to 4 carbon atoms (-CH ₂ - contained in the alkyl group is -O- or -CO- It may be substituted.), more preferably a fluorine atom, an iodine atom, a trifluoromethyl group, a methyl group, a t-butyl group, a hydroxy group, or a methoxy group.

When m2 is 0, it ^{is preferable that m8 is 1 and R 8} is a branched alkyl group having 3 or 4 carbon atoms.

If m4 is 2, preferably in the p position relative to the bonding position of R ¹ is X ^1, and is the one of the two R ⁴ on the bonding position (1 position) of the X ¹ m position and the other being a o where It is preferable that one side is 3-position, and it is more preferable that it is a bonding position whose other side is 6-position.

Examples of the cation of the salt (I) include cations represented by the following formulas (I-c-1) to (I-c-54).

[0027]

[0028]

[0029]

[0030]

[0031] ^{Examples of the organic anion represented by AI −} include a sulfonic acid anion, a sulfonylimide anion, a sulfonylmethide anion, and a carboxylate anion. AI ^- organic anions represented by is that the sulfonic acid anion is preferred, more preferably an anion represented by the formula (IA).

[In formula (I-A),

Q ¹ and Q ² each independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.

L ¹ represents a saturated hydrocarbon group having 1 to 24 carbon atoms, -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O- or -CO-, and a hydrogen atom contained in the saturated hydrocarbon group is fluorine It may be substituted with an atom or a hydroxyl group.

Y ¹ represents a methyl group which may have a substituent or an alicyclic hydrocarbon group having 3 to 24 carbon atoms which may have a substituent, and -CH ₂ - contained in the alicyclic hydrocarbon group is -O-, -SO ₂ - or - It may be substituted with CO-.]

In the formula (IA), when -CH ₂ - contained in the saturated hydrocarbon group is substituted with -O- or -C(=O)-, the number of carbon atoms before substitution is the number of carbon atoms of the saturated hydrocarbon group . _{In addition, when -CH 2} - contained in the alicyclic hydrocarbon group is substituted with -O-, -SO ₂ - or -C(=O)-, the number of carbon atoms before substitution is the number of carbon atoms in the alicyclic hydrocarbon group.

[0033] As the ^{perfluoroalkyl group having 1 to 6 carbon atoms of Q 1} and Q ² , trifluoromethyl group, perfluoroethyl group, perfluoropropyl group, perfluoroisopropyl group, perfluorobutyl group, purple A luorosec-butyl group, a perfluorotert-butyl group, a perfluoropentyl group, a perfluorohexyl group, etc. are mentioned.

Q ¹ and Q ² are, each independently, preferably a methyl group a fluorine atom or trifluoromethyl, and it is both more preferably a fluorine atom.

Examples ^{of the divalent saturated hydrocarbon group for L 1} include a linear alkanediyl group, branched alkanediyl group, monocyclic or polycyclic divalent alicyclic saturated hydrocarbon group, and at least two of these groups It may also be a contribution formed by combining .

Specifically, methylene group, ethylene group, propane-1,3-diyl group, butane-1,4-diyl group, pentane-1,5-diyl group, hexane-1,6-diyl group, heptane-1, 7-diyl group, octane-1,8-diyl group, nonane-1,9-diyl group, decane-1,10-diyl group, undecane-1,11-diyl group, dodecane-1,12-diyl group Diyl, tridecane-1,13-diyl group, tetradecane-1,14-diyl group, pentadecane-1,15-diyl group, hexadecane-1,16-diyl group and heptadecane-1,17-diyl group linear alkanediyl groups such as diaries;

Ethane-1,1-diyl group, propane-1,1-diyl group, propane-1,2-diyl group, propane-2,2-diyl group, pentane-2,4-diyl group, 2-methylpropane- branched alkanediyl groups such as 1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group, and 2-methylbutane-1,4-diyl group;

Monocyclic 2, which is a cycloalkanediyl group, such as a cyclobutane-1,3-diyl group, a cyclopentane-1,3-diyl group, a cyclohexane-1,4-diyl group, and a cyclooctane-1,5-diyl group a valent alicyclic saturated hydrocarbon group;

Polycyclic divalent alicyclics, such as norbornane-1,4-diyl group, norbornane-2,5-diyl group, adamantane-1,5-diyl group, and adamantane-2,6-diyl group A saturated hydrocarbon group etc. are mentioned.

As a _{group in which -CH 2} - contained in the divalent saturated hydrocarbon group represented by ^{L 1} is substituted with -O- or -CO-, for example, a group represented by any one of formulas (b1-1) to (b1-3) can be lifted In addition, in the group represented by the formula (b1-1) - the formula (b1-3) and the group represented by the formula (b1-4) - the formula (b1-11) which are specific examples thereof, * and ** are a binding site and * represents a binding site with ^{-Y 1 .}

[0035]

[In formula (b1-1),

L ^b2 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.

L ^b3 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group, and -CH ₂ - contained in the saturated hydrocarbon group is , -O- or -CO- may be substituted.

However, the ^{total carbon number of L b2} and L ^b3 is 22 or less.

In formula (b1-2),

L ^b4 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.

L ^b5 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group, and -CH ₂ - contained in the saturated hydrocarbon group is , -O- or -CO- may be substituted.

However, the ^{total carbon number of L b4} and L ^b5 is 22 or less.

In formula (b1-3),

L ^b6 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group.

L ^b7 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group, and -CH ₂ - contained in the saturated hydrocarbon group is , -O- or -CO- may be substituted.

However, the total number of carbon atoms of ^{L b6} and L ^{b7 is 23 or less.]}

[0036] In the group represented by formulas (b1-1) to (b1-3), when -CH ₂ - contained in the saturated hydrocarbon group is substituted with -O- or -CO-, the number of carbon atoms before substitution is Let it be the carbon number of the said saturated hydrocarbon group.

Examples of the divalent saturated hydrocarbon group include the same divalent saturated hydrocarbon group as ^{L b1 .}

L ^b2 is preferably a single bond.

L ^b3 is preferably a divalent saturated hydrocarbon group having 1 to 4 carbon atoms.

L ^b4 is preferably a divalent saturated hydrocarbon group having 1 to 8 carbon atoms, and a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom.

L ^b5 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^b6 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 4 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.

L ^b7 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group, and contained in the divalent saturated hydrocarbon group - CH ₂ - may be substituted with -O- or -CO-.

As a _{group in which -CH 2} - contained in the divalent saturated hydrocarbon group represented by ^{L 1} is substituted with -O- or -CO-, a group represented by formula (b1-1) or (b1-3) is preferable.

Examples of the group represented by the formula (b1-1) include groups represented by the formulas (b1-4) to (b1-8).

[In formula (b1-4),

L ^b8 represents a single bond or a divalent saturated hydrocarbon group having 1 to 22 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group.

In formula (b1-5),

L ^b9 represents a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and -CH ₂ - contained in the divalent saturated hydrocarbon group may be substituted with -O- or -CO-.

L ^b10 represents a single bond or a divalent saturated hydrocarbon group having 1 to 19 carbon atoms, and a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group.

However, the total carbon number of ^{L b9} and L ^{b10 is 20 or less.}

In formula (b1-6),

L ^b11 represents a divalent saturated hydrocarbon group having 1 to 21 carbon atoms.

L ^b12 represents a single bond or a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group.

However, the total carbon number of ^{L b11} and L ^{b12 is 21 or less.}

In formula (b1-7),

L ^b13 represents a divalent saturated hydrocarbon group having 1 to 19 carbon atoms.

L ^b14 represents a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and -CH ₂ - contained in the divalent saturated hydrocarbon group may be substituted with -O- or -CO-.

L ^b15 represents a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and a hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group.

However, the total number of carbon atoms of ^{L b13} to L ^{b15 is 19 or less.}

In formula (b1-8),

L ^b16 represents a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and -CH ₂ - contained in the divalent saturated hydrocarbon group may be substituted with -O- or -CO-.

L ^b17 represents a divalent saturated hydrocarbon group having 1 to 18 carbon atoms.

L ^b18 represents a single bond or a divalent saturated hydrocarbon group having 1 to 17 carbon atoms, and the hydrogen atom contained in the divalent saturated hydrocarbon group may be substituted with a fluorine atom or a hydroxyl group.

However, the total number of carbon atoms of ^{L b16} to L ^{b18 is 19 or less.]}

L ^b8 is preferably a divalent saturated hydrocarbon group having 1 to 4 carbon atoms.

L ^b9 is preferably a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^b10 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 19 carbon atoms, more preferably a single bond or a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^b11 is preferably a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^b12 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^b13 is preferably a divalent saturated hydrocarbon group having 1 to 12 carbon atoms.

L ^b14 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 6 carbon atoms.

L ^b15 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, more preferably a single bond or a divalent saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^b16 is preferably a divalent saturated hydrocarbon group having 1 to 12 carbon atoms.

L ^b17 is preferably a divalent saturated hydrocarbon group having 1 to 6 carbon atoms.

L ^b18 is preferably a single bond or a divalent saturated hydrocarbon group having 1 to 17 carbon atoms, more preferably a single bond or a divalent saturated hydrocarbon group having 1 to 4 carbon atoms.

[0038] Examples of the group represented by the formula (b1-3) include groups represented by the formulas (b1-9) to (b1-11), respectively.

[In formula (b1-9),

L ^b19 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.

L ^b20 represents a single bond or a divalent saturated hydrocarbon group having 1 to 23 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom, a hydroxyl group, or an alkylcarbonyloxy group. _{-CH 2} - contained in the alkylcarbonyloxy group may be substituted with -O- or -CO-, and the hydrogen atom contained in the alkylcarbonyloxy group may be substituted with a hydroxyl group.

However, the total carbon number of ^{L b19} and L ^{b20 is 23 or less.}

In formula (b1-10),

L ^b21 represents a single bond or a divalent saturated hydrocarbon group having 1 to 21 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.

L ^b22 represents a single bond or a divalent saturated hydrocarbon group having 1 to 21 carbon atoms.

L ^b23 represents a single bond or a divalent saturated hydrocarbon group having 1 to 21 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom, a hydroxyl group, or an alkylcarbonyloxy group. _{-CH 2} - contained in the alkylcarbonyloxy group may be substituted with -O- or -CO-, and the hydrogen atom contained in the alkylcarbonyloxy group may be substituted with a hydroxyl group.

However, the total carbon number of ^{L b21} , L ^b22 and L ^{b23 is 21 or less.}

In formula (b1-11),

L ^b24 represents a single bond or a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and a hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom.

L ^b25 represents a divalent saturated hydrocarbon group having 1 to 21 carbon atoms.

L ^b26 represents a single bond or a divalent saturated hydrocarbon group having 1 to 20 carbon atoms, and the hydrogen atom contained in the saturated hydrocarbon group may be substituted with a fluorine atom, a hydroxy group, or an alkylcarbonyloxy group. _{-CH 2} - contained in the alkylcarbonyloxy group may be substituted with -O- or -CO-, and the hydrogen atom contained in the alkylcarbonyloxy group may be substituted with a hydroxyl group.

However, the total number of carbon atoms of ^{L b24} , L ^b25 and L ^{b26 is 21 or less.]}

In addition, in the group represented by the formula (b1-9) to the group represented by the formula (b1-11), when a hydrogen atom contained in the saturated hydrocarbon group is substituted with an alkylcarbonyloxy group, the number of carbon atoms before substitution is the saturated hydrocarbon group. Let it be the number of carbon atoms in the group.

Examples of the alkylcarbonyloxy group include an acetyloxy group, a propionyloxy group, a butyryloxy group, a cyclohexylcarbonyloxy group, and an adamantylcarbonyloxy group.

Examples of the group represented by the formula (b1-4) include the following.

[0040] Examples of the group represented by the formula (b1-5) include the following.

Examples of the group represented by the formula (b1-6) include the following.

Examples of the group represented by the formula (b1-7) include the following.

Examples of the group represented by the formula (b1-8) include the following.

[0044] Examples of the group represented by the formula (b1-2) include the following.

[0045] Examples of the group represented by the formula (b1-9) include the following.

Examples of the group represented by the formula (b1-10) include the following.

[0047] Examples of the group represented by the formula (b1-11) include the following.

Examples of ^{the alicyclic hydrocarbon group represented by Y 1} include groups represented by formulas (Y1) to (Y11) and (Y36) to (Y38).

When _{-CH 2} - contained in the alicyclic hydrocarbon group represented by ^{Y 1} is substituted with -O-, -SO ₂ - or -CO-, the number may be one or two or more. As such a group, the group represented by a formula (Y12) - a formula (Y35), a formula (Y39) - a formula (Y43) is mentioned. * indicates a binding site with ^{L 1 .}

The ^{alicyclic hydrocarbon group represented by Y 1} is preferably a formula (Y1) to a formula (Y20), a formula (Y26), a formula (Y27), a formula (Y30), a formula (Y31), a formula (Y39) ) to a group represented by any one of formula (Y43), more preferably formula (Y11), formula (Y15), formula (Y16), formula (Y20), formula (Y26), formula (Y27), formula ( Y30), a group represented by a formula (Y31), a formula (Y39), a formula (Y40), a formula (Y42), or a formula (Y43), More preferably, a formula (Y11), a formula (Y15), a formula (Y20) ), a formula (Y26), a formula (Y27), a formula (Y30), a formula (Y31), a formula (Y39), a formula (Y40), a formula (Y42), or a formula (Y43).

A ^{spiro-ring in which the alicyclic hydrocarbon group represented by Y 1} has an oxygen atom of formula (Y28) to formula (Y35), formula (Y39), formula (Y40), formula (Y42) or formula (Y43) ), it is preferable that the alkanediyl group between two oxygen atoms has one or more fluorine atoms. Moreover, it is preferable that the fluorine atom is not substituted by the methylene group adjacent to an oxygen atom among the alkanediyl groups contained in a ketal structure.

Examples of the substituent of the methyl group represented by Y ¹ include a halogen atom, a hydroxyl group, an alicyclic hydrocarbon group having 3 to 16 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, a glycidyloxy group, -(CH ₂ ) _ja -CO -OR ^b1 group or -(CH ₂ ) _ja -O-CO-R ^b1 group ( ^{wherein, R b1} is an alkyl group having 1 to 16 carbon atoms, an alicyclic hydrocarbon group having 3 to 16 carbon atoms, or an aromatic group having 6 to 18 carbon atoms. represents a hydrocarbon group or a group combining them. ja represents an integer of any one of 0 to 4. -CH ₂ - included in the alkyl group and the alicyclic hydrocarbon group is -O-, -SO ₂ -, or -CO - may be substituted, and the hydrogen atom contained in this alkyl group, this alicyclic hydrocarbon group, and this aromatic hydrocarbon group may be substituted with a hydroxyl group or a fluorine atom.) etc. are mentioned.

Examples of the substituent of the alicyclic hydrocarbon group represented by Y ¹ include a halogen atom, a hydroxy group, or an alkyl group having 1 to 16 carbon atoms which may be substituted with a hydroxy group (-CH ₂ - contained in the alkyl group is -O- or -CO- may be substituted), an alicyclic hydrocarbon group having 3 to 16 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, an aralkyl group having 7 to 21 carbon atoms, a glycidyloxy group, -(CH ₂ ) _ja -CO-OR ^b1 group or -(CH ₂ ) _ja -O-CO-R ^b1 group ( ^{wherein R b1} is an alkyl group having 1 to 16 carbon atoms, an alicyclic hydrocarbon group having 3 to 16 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms, or represents a group combining these, ja represents an integer of any one of 0 to 4. -CH ₂ - contained in the alkyl group and the alicyclic hydrocarbon group is substituted with -O-, -SO _{2 - or -CO-} and the hydrogen atom contained in the said alkyl group, this alicyclic hydrocarbon group, and this aromatic hydrocarbon group may be substituted by the hydroxyl group or the fluorine atom.) etc. are mentioned.

Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

Examples of the alicyclic hydrocarbon group include a cyclopentyl group, a cyclohexyl group, a methylcyclohexyl group, a dimethylcyclohexyl group, a cycloheptyl group, a cyclooctyl group, a norbornyl group, and an adamantyl group. The alicyclic hydrocarbon group may have a chain hydrocarbon group, and a methylcyclohexyl group, a dimethylcyclohexyl group, etc. are mentioned. Carbon number of an alicyclic hydrocarbon group becomes like this. Preferably it is 3-12, More preferably, it is 3-10.

As an aromatic hydrocarbon group, aryl groups, such as a phenyl group, a naphthyl group, an anthryl group, a biphenyl group, and a phenanthryl group, etc. are mentioned, for example. The aromatic hydrocarbon group may have a chain hydrocarbon group or an alicyclic hydrocarbon group, and an aromatic hydrocarbon group having a chain hydrocarbon group having 1 to 18 carbon atoms (tolyl group, xylyl group, cumenyl group, mesityl group, p-methylphenyl group, p -ethylphenyl group, p-tert-butylphenyl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), and an aromatic hydrocarbon group having an alicyclic hydrocarbon group having 3 to 18 carbon atoms (p-cyclohexylphenyl group) , p-adamantylphenyl group, etc.) and the like. Carbon number of an aromatic hydrocarbon group becomes like this. Preferably it is 6-14, More preferably, it is 6-10.

Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, a 2-ethylhexyl group, an octyl group, a nonyl group, A decyl group, an undecyl group, a dodecyl group, etc. are mentioned. Carbon number of an alkyl group becomes like this. Preferably it is 1-12, More preferably, it is 1-6, More preferably, it is 1-4.

As an alkyl group substituted with the hydroxyl group, hydroxyalkyl groups, such as a hydroxymethyl group and a hydroxyethyl group, are mentioned.

Examples of the aralkyl group include a benzyl group, a phenethyl group, a phenylpropyl group, a naphthylmethyl group, and a naphthylethyl group.

As a group in which -CH ₂ - contained in the alkyl group is substituted with -O-, -SO ₂ - or -CO-, an alkoxy group, an alkylsulfonyl group, an alkoxycarbonyl group, an alkylcarbonyl group, an alkylcarbonyloxy group, or a combination thereof and the like.

Examples of the alkoxy group include a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentyloxy group, a hexyloxy group, a heptyloxy group, an octyloxy group, a decyloxy group, and a dodecyloxy group. Carbon number of an alkoxy group becomes like this. Preferably it is 1-12, More preferably, it is 1-6, More preferably, it is 1-4.

Examples of the alkylsulfonyl group include a methylsulfonyl group, an ethylsulfonyl group, and a propylsulfonyl group. Carbon number of an alkylsulfonyl group becomes like this. Preferably it is 1-12, More preferably, it is 1-6, More preferably, it is 1-4.

Examples of the alkoxycarbonyl group include a methoxycarbonyl group, an ethoxycarbonyl group, and a butoxycarbonyl group. Carbon number of an alkoxycarbonyl group becomes like this. Preferably it is 2-12, More preferably, it is 2-6, More preferably, it is 2-4.

Examples of the alkylcarbonyl group include an acetyl group, a propionyl group, and a butyryl group. Carbon number of an alkylcarbonyl group becomes like this. Preferably it is 2-12, More preferably, it is 2-6, More preferably, it is 2-4.

Examples of the alkylcarbonyloxy group include an acetyloxy group, a propionyloxy group, and a butyryloxy group. The number of carbon atoms of the alkylcarbonyloxy group is preferably 2 to 12, more preferably 2 to 6, still more preferably 2 to 4.

Examples of the combined group include a group combining an alkoxy group and an alkyl group, a group combining an alkoxy group and an alkoxy group, a group combining an alkoxy group and an alkylcarbonyl group, and a group combining an alkoxy group and an alkylcarbonyloxy group.

As a group combining an alkoxy group and an alkyl group, alkoxyalkyl groups, such as a methoxymethyl group, a methoxyethyl group, an ethoxyethyl group, and an ethoxymethyl group, etc. are mentioned, for example. Carbon number of an alkoxyalkyl group becomes like this. Preferably it is 2-12, More preferably, it is 2-6, More preferably, it is 2-4.

Alkoxyalkoxy groups, such as a methoxymethoxy group, a methoxyethoxy group, an ethoxymethoxy group, and an ethoxyethoxy group, etc. are mentioned as group which combined an alkoxy group and an alkoxy group. Carbon number of an alkoxyalkoxy group becomes like this. Preferably it is 2-12, More preferably, it is 2-6, More preferably, it is 2-4.

Examples of the group combining an alkoxy group and an alkylcarbonyl group include alkoxyalkylcarbonyl groups such as a methoxyacetyl group, a methoxypropionyl group, an ethoxyacetyl group and an ethoxypropionyl group. Carbon number of an alkoxyalkyl carbonyl group becomes like this. Preferably it is 3-13, More preferably, it is 3-7, More preferably, it is 3-5.

Examples of the group combining an alkoxy group and an alkylcarbonyloxy group include alkoxyalkylcarbonyloxy groups such as methoxyacetyloxy group, methoxypropionyloxy group, ethoxyacetyloxy group and ethoxypropionyloxy group. . The number of carbon atoms of the alkoxyalkylcarbonyloxy group is preferably 3 to 13, more preferably 3 to 7, still more preferably 3 to 5.

As a group in which -CH ₂ - contained in the alicyclic hydrocarbon group is substituted with -O-, -SO ₂ -, or -CO-, etc., formulas (Y12) to (Y35), (Y39) to (Y43) and the group represented.

[0052] Examples of Y ¹ include the following.

Y ¹ is preferably an alicyclic hydrocarbon group having 3 to 24 carbon atoms which may have a substituent, more preferably an alicyclic hydrocarbon group having 3 to 20 carbon atoms which may have a substituent, and still more preferably an alicyclic hydrocarbon group having 3 to 18 carbon atoms which may have a substituent, still more preferably an alicyclic hydrocarbon group substituted with a hydroxyl group, more preferably an adamantyl group which may have a substituent, and the alicyclic hydrocarbon group or _{-CH 2} - constituting the adamantyl group may be substituted with -CO-, -SO _{2 - or -CO-.} Y ¹ is specifically preferably an adamantyl group, a hydroxyadamantyl group, an oxoadamantyl group, or a group represented by the formulas (Y42), (Y100) to (Y114), and particularly preferably, hydroxy It is a group represented by an oxyadamantyl group, an oxoadamantyl group, the group containing these, or a formula (Y42), a formula (Y100) - a formula (Y114).

As the anion represented by the formula (IA), the anion represented by the formulas (IA-1) to (IA-59) [hereinafter referred to as “anion (IA-1)” according to the formula number, etc. Yes.] preferred, formulas (IA-1) to (IA-4), (IA-9), (IA-10), (IA-24) to (IA-33), formulas The anion represented by any one of (IA-36) - Formula (IA-40), Formula (IA-47) - Formula (IA-59) is more preferable.

[0055]

[0056]

[0057]

[0058]

[0059]

[0060]

[0061]

[0062] Here, R ⁱ² to R ⁱ⁷ are each independently, for example, an alkyl group having 1 to 4 carbon atoms, preferably a methyl group or an ethyl group. R ⁱ⁸ is, for example, a chain hydrocarbon group having 1 to 12 carbon atoms, preferably an alkyl group having 1 to 4 carbon atoms, an alicyclic hydrocarbon group having 5 to 12 carbon atoms, or a group formed by combining them, more preferably a methyl group or an ethyl group , a cyclohexyl group or an adamantyl group. L ^A41 is a single bond or an alkanediyl group having 1 to 4 carbon atoms. Q ¹ and Q ² have the same meanings as above.

Specifically as an anion represented by Formula (I-A), the anion of Unexamined-Japanese-Patent No. 2010-204646 is mentioned.

Preferred examples of the anion represented by the formula (I-A) include an anion represented by each of the formulas (I-a-1) to (I-a-38).

[0064]

[0065]

Among them, any one of formulas (Ia-1) to (Ia-3), (Ia-7) to (Ia-19), and (Ia-22) to (Ia-38) The anions represented are preferred.

[0067] AI ^- As the sulfonyl imide anions represented by the following.

[0068] Examples of the sulfonyl methide anion include the following.

[0069] Examples of the carboxylate anion include the following.

Specific examples of the salt (I) include a salt in which the above-described cation and anion are arbitrarily combined. Specific examples of salt (I) are shown in the table below.

In the table below, each code represents a code attached to the structure representing the above-described anion or cation, and "-" represents that each of the salt (I) and the anion (I) corresponds. For example, salt (I-1) is a salt consisting of an anion represented by formula (Ia-1) and a cation represented by formula (Ic-1), and salt (I-2) is represented by formula (Ia-2) The salt or salt (I-39) consisting of the anion represented by the anion and the cation represented by the formula (Ic-1) is a salt consisting of the anion represented by the formula (Ia-1) and the cation represented by the formula (Ic-2) indicates

[0071]

[Table 1]

Among them, salt (I) is a formula (Ia-1) to formula (Ia-4), formula (Ia-7) to formula (Ia-11), formula (Ia-14) to formula (Ia) -30) and a salt obtained by combining an anion represented by any one of formulas (Ia-35) to (Ia-38) with a cation represented by any one of formulas (Ic-1) to (Ic-54) is preferred, , specifically, salt (I-1) to salt (I-4), salt (I-7) to salt (I-11), salt (I-14) to salt (I-30), salt (I) -35) - Salt (I-38), Salt (I-39) - Salt (I-42), Salt (I-45) - Salt (I-49), Salt (I-52) - Salt (I- 68), salt (I-73) to salt (I-76), salt (I-77) to salt (I-80), salt (I-83) to salt (I-87), salt (I-90) ) to salt (I-106), salt (I-111) to salt (I-114), salt (I-115) to salt (I-118), salt (I-121) to salt (I-125) , salt (I-128) to salt (I-144), salt (I-149) to salt (I-152), salt (I-153) to salt (I-156), salt (I-159) to Salt (I-163), salt (I-166) - salt (I-182), salt (I-187) - salt (I-190), salt (I-191) - salt (I-194), salt (I-197) to salt (I-201), salt (I-204) to salt (I-220), salt (I-225) to salt (I-228), salt (I-229) to salt ( I-232), salt (I-235) to salt (I-239), salt (I-242) to salt (I-258), salt (I-263) to salt (I-266), salt (I) -267)-salt (I-270), salt (I-273)-salt (I-277), salt (I-280)-salt (I-296), salt (I-301)-salt (I- 304), salt (I-305) to salt (I-308), salt (I-311) to salt (I-315), salt (I-318) to salt (I-334), salt (I-339) ) to salt (I-342), salt (I-343) to salt (I-346), salt (I-349) to salt (I-353), salt (I-356) to salt (I-372) , salt (I-377) - salt (I-380), salt (I-381) - salt (I-384), salt (I-387) - salt (I-391), salt (I-394) - Salt (I-410), salt (I-415) to salt ( I-418), salt (I-419) - salt (I-422), salt (I-425) - salt (I-429), salt (I-432) - salt (I-448), salt (I) -453)-salt (I-456), salt (I-457)-salt (I-460), salt (I-463)-salt (I-467), salt (I-470)-salt (I- 486), salt (I-491) - salt (I-494), salt (I-495) - salt (I-498), salt (I-501) - salt (I-505), salt (I-508) ) to salt (I-524), salt (I-529) to salt (I-532), salt (I-533) to salt (I-536), salt (I-539) to salt (I-543) , salt (I-546) - salt (I-562), salt (I-567) - salt (I-570), salt (I-571) - salt (I-574), salt (I-577) - Salt (I-581), salt (I-584) - salt (I-600), salt (I-605) - salt (I-608), salt (I-609) - salt (I-612), salt (I-615) to salt (I-619), salt (I-622) to salt (I-638), salt (I-643) to salt (I-646), salt (I-647) to salt ( I-650), salt (I-653) - salt (I-657), salt (I-660) - salt (I-676), salt (I-681) - salt (I-684), salt (I) -685)-salt (I-688), salt (I-691)-salt (I-695), salt (I-698)-salt (I-714), salt (I-719)-salt (I- 722), salt (I-723) - salt (I-726), salt (I-729) - salt (I-733), salt (I-736) - salt (I-752), salt (I-757) ) to salt (I-760), salt (I-761) to salt (I-764), salt (I-767) to salt (I-771), salt (I-774) to salt (I-790) , salt (I-795) - salt (I-798), salt (I-799) - salt (I-802), salt (I-805) - salt (I-809), salt (I-812) - Salt (I-828), salt (I-833) - salt (I-836), salt (I-837) - salt (I-840), salt (I-843) - salt (I-847), salt (I-850) to salt (I-866), salt (I-871) to salt (I-874), salt (I-875) to salt (I-878), salt (I-881) to salt ( I-885), salt (I-888) - salt (I-904), salt (I-909) - salt (I-912), salt (I- 913)-salt (I-916), salt (I-919)-salt (I-923), salt (I-926)-salt (I-942), salt (I-947)-salt (I-950) ), salt (I-951) - salt (I-954), salt (I-957) - salt (I-961), salt (I-964) - salt (I-980), salt (I-985) -salt (I-988), salt (I-989) -salt (I-992), salt (I-995) -salt (I-999), salt (I-1002) -salt (I-1018), Salt (I-1023) - Salt (I-1026), Salt (I-1027) - Salt (I-1030), Salt (I-1033) - Salt (I-1037), Salt (I-1040) - Salt (I-1056), salt (I-1061) - salt (I-1064), salt (I-1065) - salt (I-1068), salt (I-1071) - salt (I-1075), salt ( I-1078) to salt (I-1094), salt (I-1099) to salt (I-1102), salt (I-1103) to salt (I-1106), salt (I-1109) to salt (I) -1113), salt (I-1116) - salt (I-1132), salt (I-1137) - salt (I-1140), salt (I-1141) - salt (I-1144), salt (I- 1147) to salt (I-1151), salt (I-1154) to salt (I-1170), salt (I-1175) to salt (I-1178), salt (I-1179) to salt (I-1182) ), salt (I-1185) - salt (I-1189), salt (I-1192) - salt (I-1208), salt (I-1213) - salt (I-1216), salt (I-1217) -salt (I-1220), salt (I-1223) -salt (I-1227), salt (I-1230) -salt (I-1246), salt (I-1251) -salt (I-1254), Salt (I-1255) - Salt (I-1258), Salt (I-1261) - Salt (I-1265), Salt (I-1268) - Salt (I-1284), Salt (I-1289) - Salt (I-1292), salt (I-1293) - salt (I-1296), salt (I-1299) - salt (I-1303), salt (I-1306) - salt (I-1322), salt ( I-1327)-salt (I-1330), salt (I-1331)-salt (I-1334), salt (I-1337)-salt (I-1341), salt (I-1344)-salt (I) -1360), salt (I-1365) - salt (I-1368), salt (I-1369) - salt (I-13) 72), salt (I-1375) to salt (I-1379), salt (I-1382) to salt (I-1398), salt (I-1403) to salt (I-1406), salt (I-1407) ) to salt (I-1410), salt (I-1413) to salt (I-1417), salt (I-1420) to salt (I-1436), salt (I-1441) to salt (I-1444) , salt (I-1445) - salt (I-1448), salt (I-1451) - salt (I-1455), salt (I-1458) - salt (I-1474), salt (I-1479) - Salt (I-1482), salt (I-1483) - salt (I-1486), salt (I-1489) - salt (I-1493), salt (I-1496) - salt (I-1512), salt (I-1517)-salt (I-1520), salt (I-1521)-salt (I-1524), salt (I-1527)-salt (I-1531), salt (I-1534)-salt ( I-1550), salt (I-1555) - salt (I-1558), salt (I-1559) - salt (I-1562), salt (I-1565) - salt (I-1569), salt (I) -1572)-salt (I-1588), salt (I-1593)-salt (I-1596), salt (I-1597)-salt (I-1600), salt (I-1603)-salt (I- 1607), salt (I-1610) - salt (I-1626), salt (I-1631) - salt (I-1634), salt (I-1635) - salt (I-1638), salt (I-1641) ) to salt (I-1645), salt (I-1648) to salt (I-1664), salt (I-1669) to salt (I-1672), salt (I-1673) to salt (I-1676) , salt (I-1679) - salt (I-1683), salt (I-1686) - salt (I-1702), salt (I-1707) - salt (I-1710), salt (I-1711) - Salt (I-1714), salt (I-1717) - salt (I-1721), salt (I-1724) - salt (I-1740), salt (I-1745) - salt (I-1748), salt (I-1749)-salt (I-1752), salt (I-1755)-salt (I-1759), salt (I-1762)-salt (I-1778), salt (I-1783)-salt ( I-1786), salt (I-1787) - salt (I-1790), salt (I-1793) - salt (I-1797), salt (I-1800) - salt (I-1816), salt (I) -1821) to salt (I-1824), salt (I-1825) ) - salt (I-1828), salt (I-1831) - salt (I-1835), salt (I-1838) - salt (I-1854), salt (I-1859) - salt (I-1862) , salt (I-1863) - salt (I-1866), salt (I-1869) - salt (I-1873), salt (I-1876) - salt (I-1892), salt (I-1897) - Salt (I-1900), salt (I-1901) - salt (I-1904), salt (I-1907) - salt (I-1911), salt (I-1914) - salt (I-1930), salt (I-1935) - Salt (I-1938), Salt (I-1939) - Salt (I-1942), Salt (I-1945) - Salt (I-1949), Salt (I-1952) - Salt ( I-1968), salt (I-1973) - salt (I-1976), salt (I-1977) - salt (I-1980), salt (I-1983) - salt (I-1987), salt (I - 1990) - Salt (I-2006), Salt (I-2011) - Salt (I-2014), Salt (I-2015) - Salt (I-2018), Salt (I-2021) - Salt (I- 2025), salts (I-2028) to salts (I-2044), and salts (I-2049) to salts (I-2052) are preferable.

[0073] <Method for producing salt (I)>

Salt (I) can be manufactured by making the salt represented by Formula (I-a) and the salt represented by Formula (I-b) react in a solvent.

[In the formula, all the symbols have the same meaning as described above, respectively. R ^A , R ^B and R ^C each independently represent a hydrocarbon group having 1 to 12 carbon atoms, or R ^A , R ^B and R ^C may be combined to form an aromatic ring. R ^D represents a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms.]

Chloroform, monochlorobenzene, acetonitrile, water etc. are mentioned as a solvent.

Reaction temperature is 15 degreeC - 80 degreeC normally, and reaction time is 0.5 to 24 hours normally.

Examples of the salt represented by the formula (I-b) include a salt represented by the following formula. These salts can be easily manufactured by the method similar to the method described in Unexamined-Japanese-Patent No. 2011-116747 and Unexamined-Japanese-Patent No. 2016-047815, or a well-known manufacturing method.

[0075] In the salt represented by the formula (Ia), R ¹ and R ² are -OL ¹ -CO-OR ^{10 The} salt (the salt represented by the formula (I-a1)) is represented by the formula (Ic) It can manufacture by making the salt represented and the compound represented by Formula (Id) react in the presence of a base catalyst in a solvent.

[In the formula, all the symbols each have the same meaning as above.]

Examples of the base include potassium carbonate, potassium iodide, pyridine, and triethylamine.

Examples of the solvent include chloroform, monochlorobenzene, dimethylformamide, acetonitrile, ethyl acetate, and water.

Reaction temperature is 15 degreeC - 80 degreeC normally, and reaction time is 0.5 to 24 hours normally.

[0076] The compound represented by the formula (I-d) includes, for example, the compounds shown below, and can be easily obtained from the market, and can also be easily produced by a known manufacturing method.

[0077] The salt represented by the formula (Ic) includes a salt represented by the formula (Ie), the compound represented by the formula (I-f1), and the compound represented by the formula (I-f2) in the presence of a catalyst , can be prepared by reacting in a solvent.

[In the formula, all the symbols each have the same meaning as above.]

As a catalyst, potassium carbonate, sodium hydride, etc. are mentioned.

Chloroform, monochlorobenzene, acetonitrile, water etc. are mentioned as a solvent.

The reaction temperature is usually 15°C to 100°C, and the reaction time is usually 0.5 to 24 hours.

[0078] Examples of the salt represented by the formula (I-e) include a salt represented by the following formula, and can be easily obtained from the market and can be easily produced by a known production method.

[0079] Examples of the compound represented by the formula (I-f1) and the compound represented by the formula (I-f2) include the compounds shown below and can be easily obtained from the market.

[0080] The salt represented by the formula (Ic) includes the salt represented by the formula (Ie), the compound represented by the formula (I-f4), and the compound represented by the formula (I-f5) of potassium carbonate It can also manufacture by making it react in presence and a solvent, and then carrying out acid treatment.

[In the formula, all the symbols have the same meaning as described above, respectively.

R ^ac represents an acid labile group.]

Chloroform, monochlorobenzene, acetonitrile, water etc. are mentioned as a solvent.

The reaction temperature is usually 15°C to 100°C, and the reaction time is usually 0.5 to 24 hours.

Examples of the acid include p-toluenesulfonic acid and hydrochloric acid.

[0081] Examples of the compound represented by the formula (I-f4) and the compound represented by the formula (I-f5) include the compounds shown below and can be easily obtained from the market.

[0082] In the salt represented by the formula (Ia), R ¹ and R ² are -OR ^{10 The} salt (the salt represented by the formula (I-a2)) is the salt represented by the formula (Ic) and the formula It can be produced by reacting the compound represented by (I-d2) in a solvent in the presence of a base catalyst.

[In the formula, all the symbols each have the same meaning as above.]

Examples of the base include sodium hydroxide and potassium hydroxide.

Examples of the solvent include chloroform, monochlorobenzene, dimethylformamide, acetonitrile, ethyl acetate, and water.

Reaction temperature is 15 degreeC - 80 degreeC normally, and reaction time is 0.5 to 24 hours normally.

[0083] The compound represented by the formula (I-d2) includes, for example, the compounds shown below, and can be easily obtained from the market, and can also be easily prepared by a known manufacturing method. .

[0084] In the salt represented by the formula (Ia), R ¹ and R ² are -O-CO-OR ^{10 The} salt (the salt represented by the formula (I-a3)) is represented by the formula (Ic) It can be produced by reacting a salt with a compound represented by formula (I-d2) in a solvent in the presence of carbonyldiimidazole.

[In the formula, all the symbols each have the same meaning as above.]

Examples of the solvent include chloroform, monochlorobenzene, dimethylformamide, acetonitrile, ethyl acetate, and water.

Reaction temperature is 15 degreeC - 80 degreeC normally, and reaction time is 0.5 to 24 hours normally.

[0085] [acid generator]

The acid generator of the present invention is an acid generator containing salt (I). One type of salt (I) may be included, and two or more types of salt (I) may be included.

The acid generator of the present invention may contain, in addition to the salt (I), an acid generator known in the resist field (hereinafter sometimes referred to as “acid generator (B)”). An acid generator (B) may be used independently and may be used in combination of 2 or more type.

[0086] The acid generator (B) may be either nonionic or ionic. Examples of the nonionic acid generator include sulfonate esters (eg, 2-nitrobenzyl ester, aromatic sulfonate, oxime sulfonate, N-sulfonyloxyimide, sulfonyloxyketone, diazonaphthoquinone 4-sulfonate); sulfones (eg, disulfone, ketosulfone, sulfonyldiazomethane); and the like. Representative examples of the ionic acid generator include onium salts containing onium cations (eg, diazonium salts, phosphonium salts, sulfonium salts, and iodonium salts). Examples of the anion of the onium salt include a sulfonic acid anion, a sulfonylimide anion, and a sulfonylmethide anion.

[0087] As the acid generator (B), Japanese Patent Application Laid-Open No. S63-26653, Japanese Patent Application Laid-Open No. S55-164824, Japanese Patent Application Laid-Open No. S62-69263, Japanese Patent Application Laid-Open No. S63-146038, Japanese Patent Laid-Open No. Radiation described in Japanese Patent Application Laid-Open No. S63-163452, Japanese Patent Application Laid-Open No. S62-153853, Japanese Patent Application Laid-Open No. S63-146029, US Patent 3,779,778, US Patent 3,849,137, German Patent No. 3914407, European Patent No. 126,712, etc. A compound that generates an acid by Moreover, you may use the compound manufactured by a well-known method. You may use an acid generator (B) in combination of 2 or more type.

The acid generator (B) is preferably a fluorine-containing acid generator, more preferably a salt represented by the formula (B1) (hereinafter referred to as “acid generator (B1)” in some cases. , except for salt (I)).

[In formula (B1),

Q ^b1 and Q ^b2 each independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.

L ^b1 represents a divalent saturated hydrocarbon group having 1 to 24 carbon atoms, -CH ₂ - contained in the divalent saturated hydrocarbon group may be substituted with -O- or -CO-, and is included in the divalent saturated hydrocarbon group The hydrogen atom to be used may be substituted with a fluorine atom or a hydroxyl group.

Y represents a methyl group which may have a substituent or an alicyclic hydrocarbon group having 3 to 24 carbon atoms which may have a substituent, and -CH ₂ - contained in the alicyclic hydrocarbon group is -O-, -SO ₂ - or -CO - may be substituted.

Z1 ⁺ represents an organic cation.]

[0089] Q ^b1 , Q ^b2 , L ^b1 and Y in Formula (B1) include the same ones as ^{Q 1} , Q ² , L ¹ and Y ¹ in Formula (IA) described above, respectively.

Examples of the sulfonic acid anion in the formula (B1) include the same as the anion represented by the formula (I-A).

Examples ^{of the organic cation of Z1+} include organic onium cations, organic sulfonium cations, organic iodonium cations, organic ammonium cations, benzothiazolium cations and organic phosphonium cations. Among these, an organic sulfonium cation and an organic iodonium cation are preferable, and an arylsulfonium cation is more preferable.

Examples ^{of the organic cation of Z +} include an organic onium cation, an organic sulfonium cation, an organic iodonium cation, an organic ammonium cation, a benzothiazolium cation, and an organic phosphonium cation. Among these, an organic sulfonium cation and an organic iodonium cation are preferable, and an arylsulfonium cation is more preferable. Specifically, a cation represented by any one of formulas (b2-1) to (b2-4) (hereinafter, depending on the formula number, may be referred to as “cation (b2-1)” or the like.) .

[0092]

In formulas (b2-1) to (b2-4),

R ^b4 to R ^b6 each independently represent a chain hydrocarbon group having 1 to 30 carbon atoms, an alicyclic hydrocarbon group having 3 to 36 carbon atoms or an aromatic hydrocarbon group having 6 to 36 carbon atoms, and a hydrogen atom contained in the chain hydrocarbon group may be substituted with a hydroxyl group, an alkoxy group having 1 to 12 carbon atoms, an alicyclic hydrocarbon group having 3 to 12 carbon atoms, or an aromatic hydrocarbon group having 6 to 18 carbon atoms, and the hydrogen atom contained in the alicyclic hydrocarbon group is a halogen atom, carbon number may be substituted with an aliphatic hydrocarbon group having 1 to 18 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms or a glycidyloxy group, and the hydrogen atom contained in the aromatic hydrocarbon group is a halogen atom, a hydroxyl group, an aliphatic hydrocarbon group having 1 to 18 carbon atoms, It may be substituted with a C1-C12 fluoroalkyl group or a C1-C12 alkoxy group.

R ^b4 and R ^b5 may combine with each other to form a ring with the sulfur atom to which they are bonded, and -CH ₂ - contained in the ring may be substituted with -O-, -S- or -CO- do.

R ^b7 and R ^b8 each independently represent a halogen atom, a hydroxyl group, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, or an alkoxy group having 1 to 12 carbon atoms.

m2 and n2 each independently represent the integer in any one of 0-5.

When m2 is 2 or more, a plurality of R ^b7 may be the same or different, and when n2 is 2 or more, a plurality of R ^b8 may be the same or different.

R ^b9 and R ^b10 each independently represent a C1-C36 chain hydrocarbon group or a C3-C36 alicyclic hydrocarbon group.

R ^b9 and R ^b10 may combine with each other to form a ring with the sulfur atom to which they are bonded, and -CH ₂ - contained in the ring may be substituted with -O-, -S- or -CO- do.

R ^b11 represents a hydrogen atom, a C1-C36 chain hydrocarbon group, a C3-C36 alicyclic hydrocarbon group, or a C6-C18 aromatic hydrocarbon group.

R ^b12 represents a chain hydrocarbon group having 1 to 12 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms or an aromatic hydrocarbon group having 6 to 18 carbon atoms, and the hydrogen atom contained in the chain hydrocarbon group is 6 to 18 carbon atoms It may be substituted with the aromatic hydrocarbon group, and the hydrogen atom contained in this aromatic hydrocarbon group may be substituted by the C1-C12 alkoxy group or the C1-C12 alkylcarbonyloxy group.

R ^b11 and R ^b12 may be bonded to each other to form a ring including -CH-CO- to which they are bonded, and -CH ₂ - contained in the ring is -O-, -S- or -CO- may be replaced with

R ^b13 to R ^b18 each independently represent a halogen atom, a hydroxyl group, an aliphatic hydrocarbon group having 1 to 12 carbon atoms, a fluorinated alkyl group having 1 to 12 carbon atoms, or an alkoxy group having 1 to 12 carbon atoms.

L ^b31 represents a sulfur atom or an oxygen atom.

o2, p2, s2, and t2 each independently represent the integer in any one of 0-5.

q2 and r2 each independently represent the integer in any one of 0-4.

u2 represents 0 or 1.

When o2 is 2 or more, a plurality of R ^b13 are the same or different, when p2 is 2 or more, a plurality of R ^b14 are the same or different, when q2 is 2 or more, a plurality of R ^b15 are the same or different, and r2 is When 2 or more, a plurality of R ^b16 are the same or different, when s2 is 2 or more, a plurality of R ^b17 are the same or different, When t2 is 2 or more, a plurality of R ^b18 are the same or different.

The aliphatic hydrocarbon group represents a chain hydrocarbon group and an alicyclic hydrocarbon group.

Examples of the chain hydrocarbon group include an alkyl group of a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, an octyl group and a 2-ethylhexyl group. .

In particular, ^{the chain hydrocarbon group of R b9} to R ^b12 preferably has 1 to 12 carbon atoms.

The alicyclic hydrocarbon group may be either monocyclic or polycyclic, and examples of the monocyclic alicyclic hydrocarbon group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, a cyclooctyl group, Cycloalkyl groups, such as a cyclodecyl group, are mentioned. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a norbornyl group, and the following groups.

In particular, ^{the alicyclic hydrocarbon group of R b9} to R ^b12 preferably has 3 to 18 carbon atoms, more preferably 4 to 12 carbon atoms.

Examples of the alicyclic hydrocarbon group in which a hydrogen atom is substituted with an aliphatic hydrocarbon group include a methylcyclohexyl group, a dimethylcyclohexyl group, a 2-methyladamantan-2-yl group, a 2-ethyladamantan-2-yl group, and a 2-isopropyla group. A dantan-2-yl group, a methyl norbornyl group, an isobornyl group, etc. are mentioned. In the alicyclic hydrocarbon group in which a hydrogen atom is substituted with an aliphatic hydrocarbon group, the total carbon number of the alicyclic hydrocarbon group and the aliphatic hydrocarbon group is preferably 20 or less.

A fluorinated alkyl group represents a C1-C12 alkyl group which has a fluorine atom, a fluoromethyl group, a difluoromethyl group, a trifluoromethyl group, perfluorobutyl, etc. are mentioned. The number of carbon atoms of the fluorinated alkyl group is preferably 1 to 9, more preferably 1 to 6, still more preferably 1 to 4.

Examples of the aromatic hydrocarbon group include an aryl group such as a phenyl group, a biphenyl group, a naphthyl group, and a phenanthryl group. The aromatic hydrocarbon group may have a chain hydrocarbon group or an alicyclic hydrocarbon group, and an aromatic hydrocarbon group having a chain hydrocarbon group having 1 to 18 carbon atoms (tolyl group, xylyl group, cumenyl group, mesityl group, p-ethylphenyl group, p -tert-butylphenyl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), and an aromatic hydrocarbon group having an alicyclic hydrocarbon group having 3 to 18 carbon atoms (p-cyclohexylphenyl group, p-adaman tylphenyl group etc.) etc. are mentioned. Moreover, when an aromatic hydrocarbon group has a chain hydrocarbon group or an alicyclic hydrocarbon group, a C1-C18 chain hydrocarbon group and a C3-C18 alicyclic hydrocarbon group are preferable.

Examples of the aromatic hydrocarbon group in which a hydrogen atom is substituted with an alkoxy group include a p-methoxyphenyl group.

Examples of the chain hydrocarbon group in which a hydrogen atom is substituted with an aromatic hydrocarbon group include aralkyl groups such as a benzyl group, a phenethyl group, a phenylpropyl group, a trityl group, a naphthylmethyl group, and a naphthylethyl group.

Examples of the alkoxy group include a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentyloxy group, a hexyloxy group, a heptyloxy group, an octyloxy group, a decyloxy group, and a dodecyloxy group.

As an alkylcarbonyl group, an acetyl group, a propionyl group, a butyryl group, etc. are mentioned.

Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

Examples of the alkylcarbonyloxy group include a methylcarbonyloxy group, an ethylcarbonyloxy group, a propylcarbonyloxy group, an isopropylcarbonyloxy group, a butylcarbonyloxy group, a sec-butylcarbonyloxy group, and a tert-butylcarbonyloxy group. A bornyloxy group, a pentylcarbonyloxy group, a hexylcarbonyloxy group, an octylcarbonyloxy group, 2-ethylhexylcarbonyloxy group, etc. are mentioned.

The ^{ring formed by combining R b4} and R ^b5 with each other to form one with the sulfur atom to which they are bonded may be any of monocyclic, polycyclic, aromatic, non-aromatic, saturated and unsaturated rings. Examples of the ring include a ring having 3 to 18 carbon atoms, and preferably a ring having 4 to 18 carbon atoms. Moreover, as for the ring containing a sulfur atom, a 3-membered ring - a 12-membered ring is mentioned, Preferably they are a 3-membered ring - a 7-membered ring, For example, the following ring is mentioned. * indicates a bond.

The ^{ring formed by combining R b9} and R b10 may be any of monocyclic, polycyclic, aromatic, non-aromatic, saturated and unsaturated rings. As for this ring, a 3-membered ring - a 12-membered ring is mentioned, Preferably it is a 3-membered ring - a 7-membered ring. For example, a thiolan-1-ium (ium) ring (tetrahydrothiophenium ring), a thian-1-ium ring, a 1,4-oxathian-4-ium ring, etc. are mentioned.

The ^{ring formed by combining R b11} and R b12 may be any of monocyclic, polycyclic, aromatic, non-aromatic, saturated and unsaturated rings. As for this ring, a 3-membered ring - a 12-membered ring is mentioned, Preferably it is a 3-membered ring - a 7-membered ring. An oxocycloheptane ring, an oxocyclohexane ring, an oxonobonane ring, an oxoadamantane ring, etc. are mentioned.

[0094] Among cations (b2-1) to cations (b2-4), cations (b2-1) are preferable.

Examples of the cation (b2-1) include the following cations.

[0095]

Examples of the cation (b2-2) include the following cations.

Examples of the cation (b2-3) include the following cations.

[0098] Examples of the cation (b2-4) include the following cations.

[0099] The acid generator (B) is a combination of the above-mentioned anion and the above-mentioned organic cation, and these may be arbitrarily combined. As acid generator (B), Preferably, Formula (B1a-1) - Formula (B1a-3), Formula (B1a-7) - Formula (B1a-16), Formula (B1a-18), Formula (B1a-) 19), a combination of an anion represented by any one of formulas (B1a-22) to (B1a-38) and a cation (b2-1), a cation (b2-3) or a cation (b2-4) is mentioned. .

[0100] The acid generator (B) preferably includes those represented by formulas (B1-1) to (B1-56), respectively. Among them, it is preferable to include an arylsulfonium cation, and formulas (B1-1) to (B1-3), (B1-5) to (B1-7), and (B1-11) to formulas ( B1-14), Formulas (B1-20) - Formula (B1-26), Formula (B1-29), Formula (B1-31) - Formula (B1-56) are especially preferable.

[0101]

[0102]

[0103]

[0104]

[0105] When salt (I) and acid generator (B) are contained as acid generators, the ratio (mass ratio) of the content of salt (I) and acid generator (B); salt (I): acid generator ( B)) is usually 1:99 to 99:1, preferably 2:98 to 98:2, more preferably 5:95 to 95:5, still more preferably 10:90 to 90 :10, and particularly preferably 15:85 to 85:15.

[0106] [resist composition]

The resist composition of the present invention contains an acid generator containing a salt (I) and a resin having an acid labile group (hereinafter sometimes referred to as “resin (A)”). Here, the "acid labile group" refers to a group having a leaving group, the leaving group is released by contact with an acid, and the structural unit is converted into a structural unit having a hydrophilic group (eg, a hydroxy group or a carboxy group).

It is preferable that the resist composition of the present invention contains a compound (hereinafter sometimes referred to as &quot;(C)&quot;) such as a salt that generates an acid having a weaker acidity than the acid generated from the acid generator. , it is preferable to contain a solvent (hereinafter sometimes referred to as "solvent (E)").

[0107] <Acid generator>

In the resist composition of the present invention, the total content of the acid generator is preferably 1 part by mass or more and 45 parts by mass or less, more preferably 1 part by mass or more and 40 parts by mass to 100 parts by mass of the resin (A) to be described later. It is a mass part or less, More preferably, they are 3 mass parts or more and 40 mass parts or less.

[0108] <Resin (A)>

Resin (A) has a structural unit having an acid-labile group (hereinafter sometimes referred to as "structural unit (a1)"). It is preferable that resin (A) contains structural units other than structural unit (a1) further. Structural units other than the structural unit (a1) include structural units having no acid-labile group (hereinafter sometimes referred to as "structural unit (s)"), structural units other than structural units (a1) and structural units (s) ( For example, a structural unit having a halogen atom (hereinafter sometimes referred to as "structural unit (a4)") described later, a structural unit having a non-leaving hydrocarbon group (hereinafter referred to as "structural unit (a5)") in some cases) and other structural units derived from monomers known in the art.

[0109] <Structural unit (a1)>

The structural unit (a1) is derived from a monomer having an acid-labile group (hereinafter sometimes referred to as “monomer (a1)”).

The acid labile group contained in the resin (A) is a group represented by the formula (1) (hereinafter also referred to as group (1)) and/or a group represented by the formula (2) (hereinafter also referred to as group (2)). ) is preferred.

[In formula (1), R ^a1 , R ^a2 and R ^a3 are each independently an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 20 carbon atoms, and 6 to 18 carbon atoms represents an aromatic hydrocarbon group or a combination thereof, or R ^a1 and R ^a2 are bonded to each other to form an alicyclic hydrocarbon group having 3 to 20 carbon atoms together with the carbon atom to which they are bonded.

ma and na each independently represent 0 or 1, and at least one of ma and na represents 1.

* indicates a bonding hand.]

[In formula (2), R ^a1' and R ^a2' each independently represent a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, and R ^a3' represents a hydrocarbon group having 1 to 20 carbon atoms, or R ^a2' and R ^a3' are bonded to each other to form a heterocyclic group having 3 to 20 carbon atoms together with the carbon atom and X to which they are bonded, and -CH ₂ - contained in the hydrocarbon group and the heterocyclic group is -O- or -S It may be replaced with -.

X represents an oxygen atom or a sulfur atom.

na' represents 0 or 1.

* indicates a bonding hand.]

[0110] Examples ^{of the alkyl group for R a1} , R ^a2 and R ^a3 include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, and an octyl group.

^Examples of the alkenyl group for R ^a1 , R ^a2 and R a3 include an ethenyl group, a propenyl group, an isopropenyl group, a butenyl group, an isobutenyl group, a tert-butenyl group, a pentenyl group, a hexenyl group, a heptenyl group, and an octynyl group. , an isooctynyl group and a nonenyl group are mentioned.

The alicyclic hydrocarbon group for R ^a1 , R ^a2 and R ^a3 may be either monocyclic or polycyclic. Examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group and a cyclooctyl group. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a norbornyl group, and the following groups (* indicates a bond). The carbon number of the alicyclic hydrocarbon group of R ^a1 , R ^a2 and R ^{a3 is preferably 3 to 16 .}

^Examples of the aromatic hydrocarbon group for R ^a1 , R ^a2 and R a3 include aryl groups such as a phenyl group, a naphthyl group, an anthryl group, a biphenyl group and a phenanthryl group.

Examples of the combined group include a group in which the above-mentioned alkyl group and an alicyclic hydrocarbon group are combined (for example, an alkylcycloalkyl group or a cycloalkylalkyl group), an aralkyl group such as a benzyl group, and an aromatic hydrocarbon group having an alkyl group (p-methylphenyl group, p-tert- butylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), an aromatic hydrocarbon group having an alicyclic hydrocarbon group (p-cyclohexylphenyl group, aryl-cycloalkyl groups such as p-adamantylphenyl group) and phenylcyclohexyl group. Preferably, ma is 0 and na is 1.

^{Examples of -C(R a1} )(R ^a2 )(R ^a3 ) when R a1 and R ^a2 combine with each other to form an alicyclic hydrocarbon group include the following groups. The alicyclic hydrocarbon group preferably has 3 to 12 carbon atoms. * represents a bond with -O-.

[0111] Examples ^{of the hydrocarbon group for R a1'} , R ^a2' and R ^a3' include an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group formed by combining these groups.

Examples of the alkyl group and the alicyclic hydrocarbon group include the same groups as those exemplified by ^{R a1} , R ^a2 and R ^{a3 .}

As an aromatic hydrocarbon group, aryl groups, such as a phenyl group, a naphthyl group, an anthryl group, a biphenyl group, and a phenanthryl group, etc. are mentioned.

Examples of the combined group include a group in which the above-mentioned alkyl group and an alicyclic hydrocarbon group are combined (for example, an alkylcycloalkyl group or a cycloalkylalkyl group), an aralkyl group such as a benzyl group, and an aromatic hydrocarbon group having an alkyl group (p-methylphenyl group, p-tert- butylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), an aromatic hydrocarbon group having an alicyclic hydrocarbon group (p-cyclohexylphenyl group, aryl-cycloalkyl groups such as p-adamantylphenyl group) and phenylcyclohexyl group.

When R ^a2' and R ^a3' combine with each other to form a hetero ring together with the carbon atom to which they are attached and X, -C(R ^a1' )(R ^a2' )-XR ^a3' includes the following groups have. * represents a bond.

It is preferable that at least one of R ^a1' and R ^{a2' is a hydrogen atom.}

na' is preferably 0.

[0112] Examples of the group (1) include the following groups.

In formula (1), R ^a1 , R ^a2 and R ^a3 are an alkyl group, ma=0, and na=1; As this group, a tert-butoxycarbonyl group is preferable.

In formula (1), R ^a1 and R ^a2 form one with the carbon atom to which they are bonded to form an adamantyl group, R ^a3 is an alkyl group, ma=0, and na=1.

In formula (1), R ^a1 and R ^a2 are each independently an alkyl group, R ^a3 is an adamantyl group, ma=0, and na=1.

Specific examples of the group (1) include the following groups. * indicates a bond.

Specific examples of the group (2) include the following groups. * indicates a bond.

[0114] The monomer (a1) is preferably a monomer having an acid labile group and an ethylenically unsaturated bond, more preferably a (meth)acrylic monomer having an acid labile group.

[0115] Among the (meth)acrylic monomers having an acid labile group, those having an alicyclic hydrocarbon group having 5 to 20 carbon atoms are preferable. When the resin (A) having a structural unit derived from a monomer (a1) having a bulky structure such as an alicyclic hydrocarbon group is used in the resist composition, the resolution of the resist pattern can be improved.

[0116] A structural unit derived from a (meth)acrylic monomer having a group (1), preferably a structural unit represented by formula (a1-0) (hereinafter referred to as structural unit (a1-0)) ), a structural unit represented by formula (a1-1) (hereinafter sometimes referred to as structural unit (a1-1)) or a structural unit represented by formula (a1-2) (hereinafter, structural unit ( a1-2) in some cases). More preferably, it is at least 1 type or 2 types of structural units selected from the group which consists of a structural unit (a1-1) and a structural unit (a1-2). These may be used independently and may use 2 or more types together.

[In formula (a1-0), formula (a1-1) and formula (a1-2),

L ^a01 , L ^a1 and L ^a2 each independently represent -O- or *-O-(CH ₂ ) _k1 -CO-O-, k1 represents an integer of any one of 1 to 7, and * is Represents a bond with -CO-.

R ^a01 , R ^a4 and R ^a5 each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.

R ^a02 , R ^a03 and R ^a04 each independently represent an alkyl group having 1 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a group combining them.

R ^a6 and R ^a7 are each independently an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a combination thereof. represents the group.

m1 represents any integer from 0 to 14.

n1 represents any integer from 0 to 10.

n1' represents any integer from 0 to 3.]

[0117] R ^a01 , R ^a4 and R ^a5 are preferably a hydrogen atom or a methyl group, more preferably a methyl group.

L ^a01 , L ^a1 and L ^a2 are preferably an oxygen atom or *-O-(CH ₂ ) _k01 -CO-O- (provided that k01 is preferably an integer of any one of 1 to 4, more Preferably it is 1.), More preferably, it is an oxygen atom.

^Examples of the alkyl group, alkenyl group, alicyclic hydrocarbon group, aromatic hydrocarbon group and combinations thereof in R a02 , R ^a03 , R ^a04 , R ^a6 and R ^{a7 include R a1} , R ^a2 and R ^{a3 in Formula (1).} The same groups as those exemplified by .

The alkyl group for R ^a02 , R ^a03 , and R ^a04 is preferably an alkyl group having 1 to 6 carbon atoms, more preferably a methyl group or an ethyl group, and still more preferably a methyl group.

The alkyl group for R ^a6 and R ^a7 is preferably an alkyl group having 1 to 6 carbon atoms, more preferably a methyl group, ethyl group, isopropyl group or t-butyl group, still more preferably an ethyl group, isopropyl group or t-butyl group.

The ^{alkenyl group for R a6} and R ^a7 is preferably an alkenyl group having 2 to 6 carbon atoms, more preferably an ethenyl group, a propenyl group, an isopropenyl group or a butenyl group.

The carbon number of the alicyclic hydrocarbon group of R ^a02 , R ^a03 , R ^a04 , R ^a6 and R ^a7 is preferably 5 to 12 , more preferably 5 to 10 .

The aromatic hydrocarbon group of R ^a02 , R ^a03 , R ^a04 , R ^a6 and R ^a7 has preferably 6 to 12 carbon atoms, more preferably 6 to 10 carbon atoms.

As for the group which combined an alkyl group and an alicyclic hydrocarbon group, it is preferable that the total carbon number which combined these alkyl group and an alicyclic hydrocarbon group is 18 or less.

As for the group which combined an alkyl group and an aromatic hydrocarbon group, it is preferable that the total carbon number which combined these alkyl group and an aromatic hydrocarbon group is 18 or less.

R ^a02 and R ^a03 are preferably an alkyl group having 1 to 6 carbon atoms or an aromatic hydrocarbon group having 6 to 12 carbon atoms, more preferably a methyl group, an ethyl group, a phenyl group or a naphthyl group.

R ^a04 is preferably an alkyl group having 1 to 6 carbon atoms or an alicyclic hydrocarbon group having 5 to 12 carbon atoms, more preferably a methyl group, an ethyl group, a cyclohexyl group or an adamantyl group.

R ^a6 and R ^a7 are preferably an alkyl group having 1 to 6 carbon atoms, an alkenyl group having 2 to 6 carbon atoms, or an aromatic hydrocarbon group having 6 to 12 carbon atoms, more preferably a methyl group, an ethyl group, an isopropyl group, or t-butyl group, an ethenyl group, a phenyl group, or a naphthyl group, more preferably an ethyl group, an isopropyl group, a t-butyl group, an ethenyl group or a phenyl group.

m1 becomes like this. Preferably it is an integer in any one of 0-3, More preferably, it is 0 or 1.

n1 becomes like this. Preferably it is an integer in any one of 0-3, More preferably, it is 0 or 1.

n1' is preferably 0 or 1.

[0118] As the structural unit (a1-0), for example, R in the structural unit and structural unit (a1-0) represented by any one of formulas (a1-0-1) to (a1-0-18) ^and structural units in which the methyl group corresponding to a01 is substituted with a hydrogen atom, a halogen atom, a haloalkyl group (an alkyl group having a halogen atom) or another alkyl group, and formulas (a1-0-1) to (a1-0-10) ), a structural unit represented by any one of formulas (a1-0-13) and (a1-0-14) is preferable.

[0119] As the structural unit (a1-1), for example, a structural unit derived from a monomer described in Japanese Patent Application Laid-Open No. 2010-204646 can be mentioned. Among these, the structural unit represented by any one of formulas (a1-1-1) to (a1-1-7) and a structure in which a methyl group corresponding to ^{R a4 in the structural unit (a1-1) is substituted with a hydrogen atom} A unit is preferable, and the structural unit represented by any one of Formula (a1-1-1) - Formula (a1-1-4) is more preferable.

^{[0120] As the structural unit (a1-2), R a5} in the structural unit and structural unit (a1-2) represented by any one of formulas (a1-2-1) to (a1-2-14) structural units in which the corresponding methyl group is substituted with a hydrogen atom, a halogen atom, a haloalkyl group or another alkyl group, formulas (a1-2-2), (a1-2-5), (a1-2-6) ) and a structural unit represented by any one of formulas (a1-2-10) to (a1-2-14) are preferable.

[0121] When the resin (A) contains the structural unit (a1-0), its content is usually 5 to 60 mol%, preferably 5 to 50 mol, based on the total structural units of the resin (A). %, and more preferably 10 to 40 mol%.

When the resin (A) contains the structural unit (a1-1) and/or the structural unit (a1-2), their total content is usually 10-95 mol% with respect to all the structural units of the resin (A). and preferably 15 to 90 mol%, more preferably 20 to 85 mol%, still more preferably 25 to 75 mol%, still more preferably 30 to 75 mol%.

[0122] As the structural unit having the group (2) in the structural unit (a1), a structural unit represented by formula (a1-4) (hereinafter referred to as “structural unit (a1-4)” in some cases.) can be heard

[In formula (a1-4),

R ^a32 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.

R ^a33 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an alkoxyalkyl group having 2 to 12 carbon atoms, an alkoxyalkoxy group having 2 to 12 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms An alkylcarbonyloxy group, acryloyloxy group or methacryloyloxy group which is 2-4 is represented.

A ^a30 silver, single bond or ^* -X ^a31 -(A ^a32 -X ^a32 ) _nc represents -, and * is -R ^a32 represents a bonding site with the carbon atom to which it is bonded.

A ^a32 represents a C1-C6 alkanediyl group.

X ^a31 and X ^a32 each independently represents -O-, -CO-O- or -O-CO-.

nc represents 0 or 1.

la represents any integer from 0 to 4. When la is any integer of 2 or more, a plurality of R ^a33 may be the same or different from each other.

R ^a34 and R ^a35 are each independently a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, R ^a36 is a hydrocarbon group having 1 to 20 carbon atoms, or R ^a35 and R ^a36 are -CO to which they are bonded Forms a divalent hydrocarbon group having 2 to 20 carbon atoms together with -, and -CH ₂ - contained in the hydrocarbon group and the divalent hydrocarbon group may be substituted with -O- or -S-.]

[0123] ^{Examples of the halogen atom in R a32} and R a33 include a fluorine atom, a chlorine atom and a bromine atom.

Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom for R ^a32 include a trifluoromethyl group, a difluoromethyl group, a methyl group, a perfluoroethyl group, a 2,2,2-trifluoroethyl group, and 1,1 ,2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group, 2,2,3,3,3-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1,2,2 ,3,3,4,4-octafluorobutyl group, butyl group, perfluoropentyl group, 2,2,3,3,4,4,5,5,5-nonafluoropentyl group, pentyl group , a hexyl group and a perfluorohexyl group.

R ^a32 is preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom, a methyl group, or an ethyl group, and still more preferably a hydrogen atom or a methyl group.

^Examples of the alkyl group for R a33 include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, and a hexyl group.

^Examples of the alkoxy group for R a33 include a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, a sec-butoxy group, a tert-butoxy group, a pentyloxy group, and a hexyloxy group. The alkoxy group is preferably an alkoxy group having 1 to 4 carbon atoms, more preferably a methoxy group or an ethoxy group, and still more preferably a methoxy group.

^Examples of the alkoxyalkyl group for R a33 include a methoxymethyl group, an ethoxyethyl group, a propoxymethyl group, an isopropoxymethyl group, a butoxymethyl group, a sec-butoxymethyl group, and a tert-butoxymethyl group. The alkoxyalkyl group is preferably an alkoxyalkyl group having 2 to 8 carbon atoms, more preferably a methoxymethyl group or an ethoxyethyl group, and still more preferably a methoxymethyl group.

^Examples of the alkoxyalkoxy group for R a33 include a methoxymethoxy group, a methoxyethoxy group, an ethoxymethoxy group, an ethoxyethoxy group, a propoxymethoxy group, an isopropoxymethoxy group, a butoxymethoxy group, sec- A butoxymethoxy group and a tert-butoxymethoxy group are mentioned. The alkoxyalkoxy group is preferably an alkoxyalkoxy group having 2 to 8 carbon atoms, more preferably a methoxyethyl group or an ethoxyethyl group.

^Examples of the alkylcarbonyl group for R a33 include an acetyl group, a propionyl group, and a butyryl group. The alkylcarbonyl group is preferably an alkylcarbonyl group having 2 to 3 carbon atoms, and more preferably an acetyl group.

^Examples of the alkylcarbonyloxy group for R a33 include an acetyloxy group, a propionyloxy group and a butyryloxy group. The alkylcarbonyloxy group is preferably an alkylcarbonyloxy group having 2 to 3 carbon atoms, and more preferably an acetyloxy group.

R ^a33 is preferably a halogen atom, a hydroxyl group, an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms, or an alkoxyalkoxy group having 2 to 8 carbon atoms, and a fluorine atom, an iodine atom, a hydroxyl group, a methyl group, a methoxy group, or an ethoxy group , an ethoxyethoxy group or an ethoxymethoxy group is more preferable, and a fluorine atom, an iodine atom, a hydroxy group, a methyl group, a methoxy group or an ethoxyethoxy group is still more preferable.

[0124] As *-X ^a31 -(A ^a32 -X ^a32 ) _nc -, *-O-, *-CO-O-, *-O-CO-, *-CO-OA ^a32 -CO-O-, *-O-CO-A ^a32 -O-, *-OA ^a32 -CO-O-, *-CO-OA ^a32 -O-CO-, *-O-CO-A ^a32 -O-CO- have. Especially, *-CO-O-, *-CO-OA ^a32 -CO-O-, or *-OA ^a32 -CO-O- is preferable.

[0125] Examples of the alkanediyl group include a methylene group, an ethylene group, a propane-1,3-diyl group, a propane-1,2-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group, Hexane-1,6-diyl group, butane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group and 2-methylbutane-1,4-diyl group.

A ^a32 is preferably a methylene group or an ethylene group.

[0126] A ^a30 is preferably a single bond, *-CO-O- or *-CO-OA ^a32 -CO-O-, a single bond, *-CO-O- or *-CO-O-CH _{It is more preferable that it is 2-} CO-O-, and it is still more preferable that it is a single bond or *-CO-O-.

[0127] la is preferably 0, 1 or 2, more preferably 0 or 1, and still more preferably 0.

^Examples of the hydrocarbon group for R a34 , R ^a35 and R ^a36 include an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group combining these groups.

Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, and an octyl group.

The alicyclic hydrocarbon group may be either monocyclic or polycyclic. Examples of the monocyclic alicyclic hydrocarbon group include cycloalkyl groups such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group and a cyclooctyl group. Examples of the polycyclic alicyclic hydrocarbon group include a decahydronaphthyl group, an adamantyl group, a norbornyl group, and the following groups (* indicates a bonding site).

As an aromatic hydrocarbon group, aryl groups, such as a phenyl group, a naphthyl group, an anthryl group, a biphenyl group, and a phenanthryl group, etc. are mentioned.

Examples of the combined group include a group in which the above-mentioned alkyl group and an alicyclic hydrocarbon group are combined (for example, an alkylcycloalkyl group or a cycloalkylalkyl group), an aralkyl group such as a benzyl group, and an aromatic hydrocarbon group having an alkyl group (p-methylphenyl group, p-tert- butylphenyl group, tolyl group, xylyl group, cumenyl group, mesityl group, 2,6-diethylphenyl group, 2-methyl-6-ethylphenyl group, etc.), an aromatic hydrocarbon group having an alicyclic hydrocarbon group (p-cyclohexylphenyl group, aryl-cycloalkyl groups such as p-adamantylphenyl group) and phenylcyclohexyl group. In particular, ^{examples of R a36} include an alkyl group having 1 to 18 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a group formed by combining these groups.

[0128] R ^a34 is preferably a hydrogen atom.

R ^a35 is preferably a hydrogen atom, an alkyl group having 1 to 12 carbon atoms, or an alicyclic hydrocarbon group having 3 to 12 carbon atoms, more preferably a methyl group or an ethyl group.

The hydrocarbon group of R ^a36 is preferably an alkyl group having 1 to 18 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a group formed by combining these, more preferably, a group formed by combining them. an alkyl group having 1 to 18 carbon atoms, an alicyclic aliphatic hydrocarbon group having 3 to 18 carbon atoms, or an aralkyl group having 7 to 18 carbon atoms. The alkyl group and the alicyclic hydrocarbon group for R ^{a36 are preferably unsubstituted.} The aromatic hydrocarbon group for R ^a36 is preferably an aromatic ring having an aryloxy group having 6 to 10 carbon atoms.

[0129] -OC(R ^a34 )(R ^a35 )-OR ^a36 in the structural unit (a1-4) comes into contact with an acid (eg p-toluenesulfonic acid) to form a hydroxyl group.

-OC(R ^a34 )(R ^a35 )-OR ^a36 is preferably bonded to the o-position or the p-position of the benzene ring, and more preferably to the p-position.

[0130] The structural unit (a1-4) includes, for example, a structural unit derived from a monomer described in Japanese Patent Application Laid-Open No. 2010-204646. Preferably, the hydrogen atom corresponding to ^{R a32} in the structural unit and structural unit (a1-4) respectively represented by formulas (a1-4-1) to (a1-4-18) is a halogen atom or halo and structural units substituted with an alkyl group or an alkyl group, and more preferably, formulas (a1-4-1) to (a1-4-5), formulas (a1-4-10), and formulas (a1-4). -13) and the structural unit respectively represented by Formula (a1-4-14) are mentioned.

[0131] When the resin (A) has a structural unit (a1-4), its content is preferably 10 to 95 mol% with respect to the total of all structural units of the resin (A), and 15 to 90 mol% It is more preferable that it is mol%, It is still more preferable that it is 20-85 mol%, It is still more preferable that it is 20-70 mol%, It is especially preferable that it is 20-60 mol%.

[0132] As the structural unit derived from the (meth)acrylic monomer having the group (2), the structural unit represented by the formula (a1-5) (hereinafter sometimes referred to as “structural unit (a1-5)”) is also can be heard

In formula (a1-5),

R ^a8 represents an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, a hydrogen atom, or a halogen atom.

Z ^a1 represents a single bond or *-(CH ₂ ) _h3 -CO-L ⁵⁴ -, h3 represents an integer of any one of 1-4, and * represents a bond with ^{L 51 .}

L ⁵¹ , L ⁵² , L ⁵³ and L ⁵⁴ each independently represent -O- or -S-.

s1 represents the integer in any one of 1-3.

s1' represents the integer in any one of 0-3.

[0133] Examples of the halogen atom include a fluorine atom and a chlorine atom, and a fluorine atom is preferable. Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a fluoromethyl group and a trifluoromethyl group.

In formula (a1-5), R ^a8 is preferably a hydrogen atom, a methyl group, or a trifluoromethyl group.

L ⁵¹ is preferably an oxygen atom.

It is preferable that one of L ⁵² and L ⁵³ is -O- and the other is -S-.

As for s1, 1 is preferable.

As for s1', the integer in any one of 0-2 is preferable.

Z ^a1 is preferably a single bond or *-CH ₂ -CO-O-.

[0134] The structural unit (a1-5) includes, for example, a structural unit derived from a monomer described in Japanese Patent Application Laid-Open No. 2010-61117. Among them, structural units represented by formulas (a1-5-1) to (a1-5-4) are preferable, and structural units represented by formulas (a1-5-1) or (a1-5-2) are preferable. A structural unit is more preferable.

[0135] When the resin (A) has a structural unit (a1-5), the content is preferably 1 to 50 mol%, and 3 to 45 mol%, based on the total structural units of the resin (A). More preferably, 5-40 mol% is still more preferable, and 5-30 mol% is still more preferable.

[0136] Further, as the structural unit (a1), the following structural units are also exemplified.

[0137] When the resin (A) contains the structural units such as (a1-3-1) to (a1-3-7) above, the content is 10 with respect to the total structural units of the resin (A). -95 mol% is preferable, 15-90 mol% is more preferable, 20-85 mol% is still more preferable, 20-70 mol% is still more preferable, 20-60 mol% is especially preferable.

[0138] <Structural unit (s)>

The structural unit (s) is derived from a monomer having no acid-labile group (hereinafter sometimes referred to as “monomer (s)”). As the monomer for deriving the structural unit (s), a monomer having no acid labile group known in the field of resists can be used.

The structural unit (s) preferably has a hydroxyl group or a lactone ring. A structural unit having a hydroxyl group and not having an acid-labile group (hereinafter sometimes referred to as “structural unit (a2)”) and/or a structural unit having a lactone ring and not having an acid-labile group (hereinafter referred to as “structural unit (a3)”) )") is used in the resist composition of the present invention, the resolution of the resist pattern and adhesion to the substrate can be improved.

[0139] <Structural unit (a2)>

The hydroxy group which the structural unit (a2) has may be an alcoholic hydroxy group or a phenolic hydroxy group.

When producing a resist pattern from the resist composition of the present invention, when high energy rays such as KrF excimer laser (248 nm), electron beam, or EUV (ultra-ultraviolet light) are used as the exposure light source, as the structural unit (a2), The structural unit (a2) which has a phenolic hydroxyl group is preferable, and it is more preferable to use the structural unit (a2-A) mentioned later. In the case of using an ArF excimer laser (193 nm) or the like, as the structural unit (a2), the structural unit (a2) having an alcoholic hydroxyl group is preferable, and it is more preferable to use the structural unit (a2-1) described later. . As a structural unit (a2), 1 type may be included individually, and 2 or more types may be included.

[0140] Examples of the structural unit having a phenolic hydroxyl group in the structural unit (a2) include a structural unit represented by formula (a2-A) (hereinafter sometimes referred to as “structural unit (a2-A)”). .

[In formula (a2-A),

R ^a50 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.

R ^a51 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an alkoxyalkyl group having 2 to 12 carbon atoms, an alkoxyalkoxy group having 2 to 12 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms, and an alkylcarbonyl group having 2 to 4 carbon atoms. An alkylcarbonyloxy group, acryloyloxy group or methacryloyloxy group which is 2-4 is represented.

A ^a50 represents a single bond or *-X ^a51 -(A ^a52 -X ^a52 ) _nb -, and * represents a bond with the carbon atom to which ^{-R a50 is bonded.}

A ^a52 represents a C1-C6 alkanediyl group.

X ^a51 and X ^a52 each independently represent -O-, -CO-O- or -O-CO-.

nb represents 0 or 1.

mb represents any integer from 0 to 4. When mb is any integer of 2 or more, a plurality of R ^a51 may be the same or different from each other.]

[0141] ^{Examples of the halogen atom in R a50} and R a51 include a fluorine atom, a chlorine atom and a bromine atom.

Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom in R ^a50 include trifluoromethyl group, difluoromethyl group, methyl group, perfluoroethyl group, 2,2,2-trifluoroethyl group, 1,1 ,2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group, 2,2,3,3,3-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1,2,2 ,3,3,4,4-octafluorobutyl group, butyl group, perfluoropentyl group, 2,2,3,3,4,4,5,5,5-nonafluoropentyl group, pentyl group , a hexyl group and a perfluorohexyl group.

R ^a50 is preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom, a methyl group or an ethyl group, and still more preferably a hydrogen atom or a methyl group.

^Examples of the alkyl group for R a51 include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, and a hexyl group. The alkyl group is preferably an alkyl group having 1 to 4 carbon atoms, more preferably a methyl group or an ethyl group, and still more preferably a methyl group.

^Examples of the alkoxy group for R a51 include a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group, a sec-butoxy group, and a tert-butoxy group. The alkoxy group is preferably an alkoxy group having 1 to 4 carbon atoms, more preferably a methoxy group or an ethoxy group, and still more preferably a methoxy group.

^Examples of the alkoxyalkyl group for R a51 include a methoxymethyl group, an ethoxyethyl group, a propoxymethyl group, an isopropoxymethyl group, a butoxymethyl group, a sec-butoxymethyl group, and a tert-butoxymethyl group. The alkoxyalkyl group is preferably an alkoxyalkyl group having 2 to 8 carbon atoms, more preferably a methoxymethyl group or an ethoxyethyl group, and still more preferably a methoxymethyl group.

^Examples of the alkoxyalkoxy group for R a51 include a methoxymethoxy group, a methoxyethoxy group, an ethoxymethoxy group, an ethoxyethoxy group, a propoxymethoxy group, an isopropoxymethoxy group, a butoxymethoxy group, sec- A butoxymethoxy group and a tert-butoxymethoxy group are mentioned. The alkoxyalkoxy group is preferably an alkoxyalkoxy group having 2 to 8 carbon atoms, and more preferably a methoxyethoxy group or an ethoxyethoxy group.

^Examples of the alkylcarbonyl group for R a51 include an acetyl group, a propionyl group and a butyryl group. The alkylcarbonyl group is preferably an alkylcarbonyl group having 2 to 3 carbon atoms, and more preferably an acetyl group.

^Examples of the alkylcarbonyloxy group for R a51 include an acetyloxy group, a propionyloxy group and a butyryloxy group. The alkylcarbonyloxy group is preferably an alkylcarbonyloxy group having 2 to 3 carbon atoms, and more preferably an acetyloxy group.

R ^a51 is preferably a halogen atom, a hydroxyl group, an alkyl group having 1 to 4 carbon atoms, an alkoxy group having 1 to 4 carbon atoms or an alkoxyalkoxy group having 2 to 8 carbon atoms, and a fluorine atom, an iodine atom, a hydroxyl group, a methyl group, a methoxy group, or an ethoxy group , an ethoxyethoxy group or an ethoxymethoxy group is more preferable, and a fluorine atom, an iodine atom, a hydroxy group, a methyl group, a methoxy group or an ethoxyethoxy group is still more preferable.

[0142] As *-X ^a51 -(A ^a52 -X ^a52 ) _nb -, *-O-, *-CO-O-, *-O-CO-, *-CO-OA ^a52 -CO-O-, *-O-CO-A ^a52 -O-, *-OA ^a52 -CO-O-, *-CO-OA ^a52 -O-CO-, *-O-CO-A ^a52 -O-CO- have. Especially, *-CO-O-, *-CO-OA ^a52 -CO-O-, or *-OA ^a52 -CO-O- is preferable.

[0143] Examples of the alkanediyl group include a methylene group, an ethylene group, a propane-1,3-diyl group, a propane-1,2-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group, Hexane-1,6-diyl group, butane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group and 2-methylbutane-1,4-diyl group.

A ^a52 is preferably a methylene group or an ethylene group.

[0144] A ^a50 is preferably a single bond, *-CO-O- or *-CO-OA ^a52 -CO-O-, and a single bond, *-CO-O- or *-CO-O-CH _{It is more preferable that it is 2-} CO-O-, and it is still more preferable that it is a single bond or *-CO-O-.

[0145] mb is preferably 0, 1 or 2, more preferably 0 or 1, particularly preferably 0.

It is preferable to couple|bond with the ortho position or para position of a benzene ring, and, as for a hydroxyl group, it is more preferable to couple|bond with para position.

[0146] Examples of the structural unit (a2-A) include structural units derived from monomers described in Japanese Patent Application Laid-Open Nos. 2010-204634 and 2012-12577.

Examples of the structural unit (a2-A) include structural units represented by formulas (a2-2-1) to (a2-2-16) and formulas (a2-2-1) to (a2-2-16). ^{Structural units in which the methyl group corresponding to R a50} in the structural unit (a2-A) in the structural unit represented is substituted with a hydrogen atom, a halogen atom, a haloalkyl group or another alkyl group is exemplified. The structural unit (a2-A) is a structural unit represented by a formula (a2-2-1), a structural unit represented by a formula (a2-2-3), or a structural unit represented by a formula (a2-2-6) , a structural unit represented by a formula (a2-2-8), a structural unit represented by a formula (a2-2-12) to a formula (a2-2-14), and a structure represented by a formula (a2-2-1) unit, the structural unit represented by the formula (a2-2-3), the structural unit represented by the formula (a2-2-6), the structural unit represented by the formula (a2-2-8), the structural unit represented by the formula (a2-2- 12) in the structural unit represented by the formula (a2-2-14), preferably a structural unit in which ^{a methyl group corresponding to R a50} in the structural unit (a2-A) is substituted with a hydrogen atom; Structural unit represented by -2-3), structural unit represented by formula (a2-2-8), structural unit represented by formula (a2-2-12) to formula (a2-2-14), and formula ( In the structural unit represented by a2-2-3) or the structural unit represented by the formula (a2-2-8), and the structural unit represented by the formulas (a2-2-12) to (a2-2-14), ^{, more preferably a structural unit in which the methyl group corresponding to R a50} in the structural unit (a2-A) is substituted with a hydrogen atom, the structural unit represented by the formula (a2-2-8) and the formula (a2-2- In the structural unit represented by 8), it is more preferable that the methyl group corresponding to ^{R a50 in the structural unit (a2-A) is substituted with a hydrogen atom.}

[0147] When the structural unit (a2-A) is included in the resin (A), the content of the structural unit (a2-A) is preferably 5 to 80 mol%, more preferably, with respect to the total structural units. is 10 to 70 mol%, more preferably 15 to 65 mol%, still more preferably 20 to 65 mol%.

The structural unit (a2-A) can be included in the resin (A) by, for example, polymerizing using the structural unit (a1-4) and then treating with an acid such as p-toluenesulfonic acid. In addition, the structural unit (a2-A) can be included in the resin (A) by performing polymerization using acetoxystyrene or the like, followed by treatment with an alkali such as tetramethylammonium hydroxide.

[0148] Examples of the structural unit having an alcoholic hydroxyl group in the structural unit (a2) include a structural unit represented by the formula (a2-1) (hereinafter sometimes referred to as “structural unit (a2-1)”). have.

In formula (a2-1),

L ^a3 represents -O- or *-O-(CH ₂ ) _k2 -CO-O-,

k2 represents the integer in any one of 1-7. * represents a bond with -CO-.

R ^a14 represents a hydrogen atom or a methyl group.

R ^a15 and R ^a16 each independently represent a hydrogen atom, a methyl group, or a hydroxy group.

o1 represents the integer in any one of 0-10.

[0149] In formula (a2-1), L ^a3 is preferably -O-, -O-(CH ₂ ) _f1 -CO-O- (wherein f1 is an integer of any one of 1 to 4) ), more preferably -O-.

R ^a14 is preferably a methyl group.

R ^a15 is preferably a hydrogen atom.

R ^a16 is preferably a hydrogen atom or a hydroxy group.

o1 is preferably the integer in any one of 0-3, More preferably, it is 0 or 1.

[0150] The structural unit (a2-1) includes, for example, a structural unit derived from a monomer described in Japanese Patent Application Laid-Open No. 2010-204646. A structural unit represented by any one of formulas (a2-1-1) to (a2-1-6) is preferable, and a structural unit represented by any one of formulas (a2-1-1) to (a2-1-4) A structural unit is more preferable, and the structural unit represented by a formula (a2-1-1) or a formula (a2-1-3) is still more preferable.

[0151] When the resin (A) contains the structural unit (a2-1), its content is usually 1 to 45 mol%, preferably 1 to 40 mol, based on the total structural units of the resin (A). %, more preferably 1-35 mol%, still more preferably 1-20 mol%, still more preferably 1-10 mol%.

[0152] <Structural unit (a3)>

The lactone ring of the structural unit (a3) may be a monocyclic such as a β-propiolactone ring, a γ-butyrolactone ring, or a δ-valerolactone ring, or a condensed ring of a monocyclic lactone ring and another ring. do. Preferably, a γ-butyrolactone ring, an adamantanlactone ring, or a bridged ring containing a γ-butyrolactone ring structure (eg, a structural unit represented by the following formula (a3-2)) is mentioned. can

[0153] The structural unit (a3) is preferably a structural unit represented by the formula (a3-1), the formula (a3-2), the formula (a3-3), or the formula (a3-4). Among these, 1 type may be contained individually, and 2 or more types may be contained.

[In formula (a3-1), formula (a3-2), formula (a3-3) and formula (a3-4),

L ^a4 , L ^a5 and L ^a6 are each independently represented by -O- or *-O-(CH ₂ ) _k3 -CO-O- (k3 represents an integer of any one of 1 to 7) represents the group.

L ^a7 is -O-, *-OL ^a8 -O-, *-OL ^a8 -CO-O-, *-OL ^a8 -CO-OL ^a9 -CO-O- or *-OL ^a8 -O-CO- ^Represents L a9 -O-.

L ^a8 and L ^a9 each independently represent an alkanediyl group having 1 to 6 carbon atoms.

* indicates a binding site with a carbonyl group.

R ^a18 , R ^a19 and R ^a20 each independently represent a hydrogen atom or a methyl group.

R ^a24 represents an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, a hydrogen atom, or a halogen atom.

X ^a3 represents -CH ₂ - or an oxygen atom.

R ^a21 represents an aliphatic hydrocarbon group having 1 to 4 carbon atoms.

R ^a22 , R ^a23 and R ^a25 each independently represent a carboxy group, a cyano group, or an aliphatic hydrocarbon group having 1 to 4 carbon atoms.

p1 represents the integer in any one of 0-5.

q1 represents the integer in any one of 0-3.

r1 represents the integer in any one of 0-3.

w1 represents the integer in any one of 0-8.

When p1, q1, r1 and/or w1 is 2 or more, a plurality of R ^a21 , R ^a22 , R ^a23 and/or R ^a25 may be the same as or different from each other.]

[0154] ^{Examples of the aliphatic hydrocarbon group for R a21} , R ^a22 , R ^a23 and R a25 include an alkyl group such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group and a tert-butyl group. can

^Examples of the halogen atom for R a24 include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

^Examples of the alkyl group for R a24 include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group and a hexyl group, preferably having 1 to 4 carbon atoms. A phosphorus alkyl group is mentioned, More preferably, a methyl group or an ethyl group is mentioned.

^Examples of the alkyl group having a halogen atom for R a24 include a trifluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluoroisopropyl group, a perfluorobutyl group, a perfluorosec-butyl group, and a purple group. Luorotert-butyl group, perfluoropentyl group, perfluorohexyl group, trichloromethyl group, tribromomethyl group, triiodomethyl group, etc. are mentioned.

^Examples of the alkanediyl group for L ^a8 and L a9 include a methylene group, an ethylene group, a propane-1,3-diyl group, a propane-1,2-diyl group, a butane-1,4-diyl group, a pentane-1, 5-diyl group, hexane-1,6-diyl group, butane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1 and a ,4-diyl group and a 2-methylbutane-1,4-diyl group.

[0155] In formulas (a3-1) to (a3-3), L ^a4 to L ^a6 are each independently, preferably -O- or *-O-(CH ₂ ) _k3 -CO- In O-, k3 is an integer of any one of 1 to 4, more preferably -O- and *-O-CH ₂ -CO-O-, still more preferably an oxygen atom.

R ^a18 to R ^a21 are preferably a methyl group.

R ^a22 and R ^a23 are each independently, preferably a carboxy group, a cyano group, or a methyl group.

p1, q1, and r1 are each independently, Preferably it is an integer in any one of 0-2, More preferably, it is 0 or 1.

[0156] In formula (a3-4), R ^a24 is preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom, a methyl group or an ethyl group, and still more preferably a hydrogen atom or a methyl group. am.

R ^a25 is preferably a carboxy group, a cyano group or a methyl group.

L ^a7 is preferably -O- or *-OL ^a8 -CO-O-, more preferably -O-, -O-CH ₂ -CO-O- or -OC ₂ H ₄ -CO-O -am.

w1 becomes like this. Preferably it is an integer in any one of 0-2, More preferably, it is 0 or 1.

In particular, the formula (a3-4) is preferably a formula (a3-4)'.

(In the formula, R ^a24 and L ^a7 have the same meanings as above.)

[0157] The structural unit (a3) is derived from the monomer described in Japanese Patent Application Laid-Open No. 2010-204646, the monomer described in Japanese Patent Application Laid-Open No. 2000-122294, and the monomer described in Japanese Patent Laid-Open No. 2012-41274. structural units are mentioned. As the structural unit (a3), formula (a3-1-1), formula (a3-1-2), formula (a3-2-1), formula (a3-2-2), formula (a3-3-1) ), a structural unit represented by any one of formulas (a3-3-2) and (a3-4-1) to (a3-4-12), and in the structural unit, formulas (a3-1) to is a methyl group corresponding to R ^a18, R ^a19, R ^a20 and R ^a24 in the formula (a3-4) is preferably a structural unit substituted with hydrogen atoms.

[0158]

[0159] When the resin (A) contains the structural unit (a3), the total content thereof is usually 5 to 70 mol%, preferably 10 to 65 mol%, based on all the structural units of the resin (A). and more preferably 10 to 60 mol%.

In addition, the content rate of a structural unit (a3-1), a structural unit (a3-2), a structural unit (a3-3), or a structural unit (a3-4) with respect to all the structural units of resin (A), respectively, 5-60 mol% is preferable, 5-50 mol% is more preferable, 10-50 mol% is still more preferable.

[0160] <Structural unit (a4)>

Examples of the structural unit (a4) include the following structural units.

[in formula (a4),

R ⁴¹ represents a hydrogen atom or a methyl group.

R ⁴² represents a saturated hydrocarbon group having a fluorine atom having 1 to 24 carbon atoms, and -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O- or -CO-.]

Examples of the saturated hydrocarbon group represented by R ⁴² include a chain hydrocarbon group, a monocyclic or polycyclic alicyclic hydrocarbon group, and a group formed by combining these groups.

[0161] Examples of the chain hydrocarbon group include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a decyl group, a dodecyl group, a pentadecyl group, a hexadecyl group, a heptadecyl group, and an octadecyl group. decyl group. Examples of the monocyclic or polycyclic alicyclic hydrocarbon group include cycloalkyl groups such as cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl; and polycyclic alicyclic hydrocarbon groups such as a decahydronaphthyl group, an adamantyl group, a norbornyl group, and the following groups (* represents a bond).

Examples of the group formed by the combination include a group formed by combining one or more alkyl groups or one or more alkanediyl groups and one or more alicyclic hydrocarbon groups, -alkanediyl group-alicyclic hydrocarbon group, -alicyclic hydrocarbon group- An alkyl group, -alkanediyl group-alicyclic hydrocarbon group-alkyl group, etc. are mentioned.

[0162] The structural unit (a4) is selected from the group consisting of formula (a4-0), formula (a4-1), formula (a4-2), formula (a4-3) and formula (a4-4) The structural unit represented by at least 1 is mentioned.

[In formula (a4-0),

R ⁵ represents a hydrogen atom or a methyl group.

L ^4a represents a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 4 carbon atoms.

L ^3a represents a perfluoroalkanediyl group having 1 to 8 carbon atoms or a perfluorocycloalkanediyl group having 3 to 12 carbon atoms.

R ⁶ represents a hydrogen atom or a fluorine atom.]

[0163] Examples ^{of the divalent aliphatic saturated hydrocarbon group for L 4a} include a straight-chain alkanediyl group such as a methylene group, an ethylene group, a propane-1,3-diyl group, and a butane-1,4-diyl group, and ethane-1 Branching of 1-diyl group, propane-1,2-diyl group, butane-1,3-diyl group, 2-methylpropane-1,3-diyl group and 2-methylpropane-1,2-diyl group A shape alkanediyl group is mentioned.

Examples of the perfluoroalkanediyl group for L ^3a include a difluoromethylene group, a perfluoroethylene group, a perfluoropropane-1,1-diyl group, a perfluoropropane-1,3-diyl group, and a perfluoro lopropane-1,2-diyl group, perfluoropropane-2,2-diyl group, perfluorobutane-1,4-diyl group, perfluorobutane-2,2-diyl group, perfluorobutane -1,2-diyl group, perfluoropentane-1,5-diyl group, perfluoropentane-2,2-diyl group, perfluoropentane-3,3-diyl group, perfluorohexane-1 ,6-diyl group, perfluorohexane-2,2-diyl group, perfluorohexane-3,3-diyl group, perfluoroheptane-1,7-diyl group, perfluoroheptane-2,2 -diyl group, perfluoroheptane-3,4-diyl group, perfluoroheptane-4,4-diyl group, perfluorooctane-1,8-diyl group, perfluorooctane-2,2-di diyl, perfluorooctane-3,3-diyl group, perfluorooctane-4,4-diyl group, etc. are mentioned.

^Examples of the perfluorocycloalkanediyl group for L 3a include a perfluorocyclohexanediyl group, a perfluorocyclopentanediyl group, a perfluorocycloheptanediyl group, and a perfluoroadamantanediyl group.

[0164] L ^4a is preferably a single bond, a methylene group, or an ethylene group, and more preferably a single bond or a methylene group.

L ^3a is preferably a perfluoroalkanediyl group having 1 to 6 carbon atoms, and more preferably a perfluoroalkanediyl group having 1 to 3 carbon atoms.

[0165] Examples of the structural unit (a4-0) include the structural units shown below and structural units in ^{which the methyl group corresponding to R 5} in the structural unit (a4-0) in the following structural units is substituted with a hydrogen atom.

[0166]

[In formula (a4-1),

R ^a41 represents a hydrogen atom or a methyl group.

R ^a42 represents a saturated hydrocarbon group having 1 to 20 carbon atoms which may have a substituent, and -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O- or -CO-.

A ^a41 represents a C1-C6 alkanediyl group which may have a substituent, or group represented by a formula (a-g1). However, ^{at least one of A a41} and R ^a42 has a halogen atom (preferably a fluorine atom) as a substituent.

[in formula (a-g1),

s represents 0 or 1.

^{A42 a44} A and A each independently represents a 1 to 5 carbon atoms in the divalent saturated hydrocarbon group which may have a substituent.

A ^a43 represents a single bond or a divalent aliphatic hydrocarbon group having 1 to 5 carbon atoms which may have a substituent.

X ^a41 and X ^a42 each independently represent -O-, -CO-, -CO-O- or -O-CO-.

However, A ^a42, A ^{a43, a44} A, the sum of carbon atoms in X and X ^{a41 a42} is 7 or less.]

* is a bond, and * on the right is a bond with -O-CO-R ^a42 .]

[0167] ^Examples of the saturated hydrocarbon group for R a42 include a linear saturated hydrocarbon group, a monocyclic or polycyclic alicyclic saturated hydrocarbon group, and a group formed by combining these groups.

Examples of the saturated chain hydrocarbon group include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a decyl group, a dodecyl group, a pentadecyl group, a hexadecyl group, a heptadecyl group and an octadecyl group. can be heard

Examples of the monocyclic or polycyclic alicyclic hydrocarbon group include cycloalkyl groups such as cyclopentyl, cyclohexyl, cycloheptyl and cyclooctyl; and polycyclic alicyclic saturated hydrocarbon groups such as a decahydronaphthyl group, an adamantyl group, a norbornyl group, and the following groups (* represents a bond).

Examples of the group formed by the combination include a group formed by combining one or more alkyl groups or one or more alkanediyl groups and one or more alicyclic saturated hydrocarbon groups, -alkanediyl group-alicyclic saturated hydrocarbon group, -alicyclic saturated hydrocarbon group-alkyl group, -alkanediyl group-alicyclic saturated hydrocarbon group-alkyl group, etc. are mentioned.

[0168] ^Examples of the substituent R a42 may have include at least one selected from a halogen atom and a group represented by the formula (a-g3). Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom, and a fluorine atom is preferable.

[In formula (a-g3),

X ^a43 represents an oxygen atom, a carbonyl group, *-O-CO- or *-CO-O-.

A ^a45 represents an aliphatic hydrocarbon group having 1 to 17 carbon atoms which may have a halogen atom. * indicates a bond with ^{R a42.]}

However, in the -X ^a42 R ^a43 -A ^a45, R ^a42, if does not have a halogen atom, A is ^a45, at least one represents a group having a carbon number of an aliphatic hydrocarbon having 1 to 17 halogen atoms.

[0169] ^Examples of the aliphatic hydrocarbon group for A a45 include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, a heptyl group, an octyl group, a decyl group, a dodecyl group, a pentadecyl group, a hexadecyl group, and a heptyl group. Alkyl groups, such as a tadecyl group and an octadecyl group; monocyclic alicyclic hydrocarbon groups such as a cyclopentyl group, a cyclohexyl group, a cycloheptyl group, and a cyclooctyl group; and polycyclic alicyclic hydrocarbon groups such as decahydronaphthyl group, adamantyl group, norbornyl group, and the following groups (* represents a bond).

Examples of the group formed by the combination include a group formed by combining one or more alkyl groups or one or more alkanediyl groups and one or more alicyclic hydrocarbon groups, -alkanediyl group-alicyclic hydrocarbon group, -alicyclic hydrocarbon group- An alkyl group, -alkanediyl group-alicyclic hydrocarbon group-alkyl group, etc. are mentioned.

[0170] R ^a42 is preferably an aliphatic hydrocarbon group which may have a halogen atom, more preferably an alkyl group having a halogen atom and/or an aliphatic hydrocarbon group having a group represented by formula (a-g3).

When R ^a42 is an aliphatic hydrocarbon group having a halogen atom, it is preferably an aliphatic hydrocarbon group having a fluorine atom, more preferably a perfluoroalkyl group or a perfluorocycloalkyl group, still more preferably having 1 to 6 carbon atoms. It is a perfluoroalkyl group, Especially preferably, it is a C1-C3 perfluoroalkyl group. Examples of the perfluoroalkyl group include a perfluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluorobutyl group, a perfluoropentyl group, a perfluorohexyl group, a perfluoroheptyl group, and a perfluorooxy group. til group etc. are mentioned. As a perfluorocycloalkyl group, a perfluorocyclohexyl group etc. are mentioned.

When R ^a42 is an aliphatic hydrocarbon group having a group represented by the formula (a-g3), the total number of carbon atoms in ^{R a42} including the number of carbon atoms contained in the group represented by the formula (a-g3) is preferably 15 or less, 12 or less are more preferable. When it has the group represented by a formula (a-g3) as a substituent, one is preferable for the number.

[0171] When R ^a42 is an aliphatic hydrocarbon having a group represented by formula (a-g3), R ^a42 is more preferably a group represented by formula (a-g2).

[In formula (a-g2),

A ^a46 represents a divalent aliphatic hydrocarbon group having 1 to 17 carbon atoms which may have a halogen atom.

X ^a44 represents **-O-CO- or **-CO-O- (** represents a bond with ^{A a46 ).}

A ^a47 represents an aliphatic hydrocarbon group having 1 to 17 carbon atoms which may have a halogen atom.

However, the total number of carbon atoms of ^{A a46} , A ^a47 and X ^{a44 is 18 or less, and at least one of A a46} and A ^a47 has at least one halogen atom.

* indicates a bond with a carbonyl group.]

[0172] ^{The number of carbon atoms of the aliphatic hydrocarbon group of A a46} is preferably 1 to 6, more preferably 1 to 3.

^4-15 are preferable, as for carbon number of the aliphatic hydrocarbon group of A ^a47 , 5-12 are more preferable, and, as for A a47, a cyclohexyl group or an adamantyl group is still more preferable.

[0173] A preferable structure of the group represented by the formula (a-g2) is the following structure (* is a bond with a carbonyl group).

[0174] ^Examples of the alkanediyl group for A a41 include a methylene group, an ethylene group, a propane-1,3-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group, hexane-1, straight-chain alkanediyl groups such as 6-diyl groups; Propane-1,2-diyl group, butane-1,3-diyl group, 2-methylpropane-1,2-diyl group, 1-methylbutane-1,4-diyl group, 2-methylbutane-1,4 - branched alkanediyl groups, such as a diyl group, are mentioned.

As ^{a substituent in the alkanediyl group of A a41} , a hydroxyl group, a C1-C6 alkoxy group, etc. are mentioned.

A ^a41 is preferably an alkanediyl group having 1 to 4 carbon atoms, more preferably an alkanediyl group having 2 to 4 carbon atoms, still more preferably an ethylene group.

[0175] formula (a-g1) indicated that groups A ^a42, A ^a43 and A ^a44 represents a divalent saturated hydrocarbon group includes straight chain or branched alkanediyl group and a divalent alicyclic hydrocarbon group of a monocyclic according to, and and a group formed by combining an alkanediyl group and a divalent alicyclic hydrocarbon group. Specifically, a methylene group, an ethylene group, a propane-1,3-diyl group, a propane-1,2-diyl group, a butane-1,4-diyl group, a 1-methylpropane-1,3-diyl group, 2 -methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, etc. are mentioned.

Examples A ^a42, A ^a43 and ^a44 A represents a substituent of the divalent saturated hydrocarbon group, and the like can be mentioned a hydroxyl group and having 1 to 6 carbon atoms in the alkoxy group.

It is preferable that s is 0.

[0176] In the group represented by the formula (a-g1), examples of the group in which X ^a42 is -O-, -CO-, -CO-O- or -O-CO- include the following groups. In the following examples, * and ** each represent a bond, and ** is a bond with -O-CO-R ^a42 .

[0177] As the structural unit represented by formula (a4-1), a methyl group corresponding to ^{R a41} in the structural unit represented by formula (a4-1) in the structural units and structural units shown below is substituted with a hydrogen atom structural units can be mentioned.

[0178]

[0179] As the structural unit represented by the formula (a4-1), the structural unit represented by the formula (a4-2) is preferable.

[In formula (a4-2),

R ^f5 represents a hydrogen atom or a methyl group.

L ⁴⁴ represents an alkanediyl group having 1 to 6 carbon atoms, and -CH ₂ - contained in the alkanediyl group may be substituted with -O- or -CO-.

R ^f6 represents a saturated hydrocarbon group having a fluorine atom having 1 to 20 carbon atoms.

However, the upper limit of the total number of carbon atoms of ^{L 44} and R ^{f6 is 21.]}

[0180] Examples of the alkanediyl group having 1 to 6 carbon atoms in ^{L 44} include the same groups as those exemplified as the alkanediyl group in ^{A a41 .}

Examples of the saturated hydrocarbon group for R ^f6 include the same groups as those exemplified by ^{R a42 .}

Al as the alkanediyl group having 1 to 6 carbon atoms in the L ^44, a carbon number of 2 to 4 alkanediyl group is preferred, and more preferably an ethylene group.

[0181] Examples of the structural unit represented by formula (a4-2) include structural units represented by formulas (a4-1-1) to (a4-1-11), respectively. A structural unit in which the ^{methyl group corresponding to R f5} in the structural unit (a4-2) is substituted with a hydrogen atom is also exemplified as the structural unit represented by the formula (a4-2).

[0182] Examples of the structural unit (a4) include a structural unit represented by formula (a4-3).

[In formula (a4-3),

R ^f7 represents a hydrogen atom or a methyl group.

L ⁵ represents an alkanediyl group having 1 to 6 carbon atoms.

A ^f13 represents a divalent saturated hydrocarbon group having 1 to 18 carbon atoms which may have a fluorine atom.

X ^f12 represents *-O-CO- or *-CO-O- (* represents a bond with ^{A f13 ).}

A ^f14 represents a C1-C17 saturated hydrocarbon group which may have a fluorine atom.

However, ^{at least one of A f13} and A ^f14 has a fluorine atom, and the upper limit of the total carbon number of ^{L 5} , A ^f13 and A ^{f14 is 20.]}

[0183] Examples of the alkanediyl group for ^{L 5} include the same groups as those exemplified as the alkanediyl group in the divalent saturated hydrocarbon group of ^{A a41 .}

The ^{divalent saturated hydrocarbon group which may have a fluorine atom in A f13} is preferably a divalent aliphatic saturated hydrocarbon group which may have a fluorine atom and a divalent alicyclic saturated hydrocarbon group which may have a fluorine atom, more Preferably, it is a perfluoro alkanediyl group.

As a divalent aliphatic hydrocarbon group which may have a fluorine atom, Alkanediyl groups, such as a methylene group, an ethylene group, a propanediyl group, a butanediyl group, and a pentanediyl group; and perfluoroalkanediyl groups such as difluoromethylene group, perfluoroethylene group, perfluoropropanediyl group, perfluorobutanediyl group and perfluoropentanediyl group.

The divalent alicyclic hydrocarbon group which may have a fluorine atom may be either monocyclic or polycyclic. Examples of the monocyclic group include a cyclohexanediyl group and a perfluorocyclohexanediyl group. Examples of the polycyclic group include an adamantanediyl group, a norbornanediyl group, and a perfluoroadamantanediyl group.

Examples of the saturated hydrocarbon group of A ^{f14 and} the saturated hydrocarbon group which may have a fluorine atom include the same groups as those exemplified by ^{R a42 .} Among them, trifluoromethyl group, difluoromethyl group, methyl group, perfluoroethyl group, 2,2,2-trifluoroethyl group, 1,1,2,2-tetrafluoroethyl group, ethyl group, perfluoropropyl group group, 2,2,3,3,3-pentafluoropropyl group, propyl group, perfluorobutyl group, 1,1,2,2,3,3,4,4-octafluorobutyl group, butyl group, perfluoropentyl group, 2,2,3,3,4,4,5,5,5-nonafluoropentyl group, pentyl group, hexyl group, perfluorohexyl group, heptyl group, perfluoro Fluorinated alkyl groups such as heptyl group, octyl group and perfluorooctyl group, cyclopropylmethyl group, cyclopropyl group, cyclobutylmethyl group, cyclopentyl group, cyclohexyl group, perfluorocyclohexyl group, adamantyl group, adamantyl group A methyl group, an adamantyldimethyl group, a norbornyl group, a norbornylmethyl group, a perfluoro adamantyl group, a perfluoro adamantyl methyl group, etc. are preferable.

[0184] In formula (a4-3), L ⁵ is preferably an ethylene group.

The ^{divalent saturated hydrocarbon group of A f13} is preferably a group containing a divalent chain hydrocarbon group having 1 to 6 carbon atoms and a divalent alicyclic hydrocarbon group having 3 to 12 carbon atoms, more preferably a divalent chain hydrocarbon group having 2 to 3 carbon atoms. desirable.

The saturated hydrocarbon group of A ^f14 is preferably a group containing a chain hydrocarbon group having 3 to 12 carbon atoms and an alicyclic hydrocarbon group having 3 to 12 carbon atoms, and a chain hydrocarbon group having 3 to 10 carbon atoms and an alicyclic hydrocarbon group having 3 to 10 carbon atoms. A group comprising a group is more preferred. Among them, A ^f14 is preferably a group containing an alicyclic hydrocarbon group having 3 to 12 carbon atoms, more preferably a cyclopropylmethyl group, a cyclopentyl group, a cyclohexyl group, a norbornyl group, and an adamantyl group.

[0185] Examples of the structural unit represented by formula (a4-3) include structural units represented by formulas (a4-1'-1) to (a4-1'-11), respectively. A structural unit in which the ^{methyl group corresponding to R f7} in the structural unit (a4-3) is substituted with a hydrogen atom is also exemplified as the structural unit represented by the formula (a4-3).

[0186] Examples of the structural unit (a4) include a structural unit represented by formula (a4-4).

[In formula (a4-4),

R ^f21 represents a hydrogen atom or a methyl group.

A ^f21 represents -(CH ₂ ) _j1 -, -(CH ₂ ) _j2 -O-(CH ₂ ) _j3 - or -(CH ₂ ) _j4 -CO-O-(CH ₂ ) _j5 -.

j1 to j5 each independently represent the integer in any one of 1-6.

R ^f22 represents a saturated hydrocarbon group having 1 to 10 carbon atoms and having a fluorine atom.]

[0187] ^Examples of the saturated hydrocarbon group of R f22 are the same as the saturated hydrocarbon group represented by ^{R a42.} R ^f22 is preferably an alkyl group having 1 to 10 carbon atoms having a fluorine atom or an alicyclic hydrocarbon group having 1 to 10 carbon atoms having a fluorine atom, more preferably an alkyl group having 1 to 10 carbon atoms having a fluorine atom, and having a fluorine atom An alkyl group having 1 to 6 carbon atoms is more preferable.

[0188] In the formula (a4-4), as A ^f21 , -(CH ₂ ) _j1 - is preferable, an ethylene group or a methylene group is more preferable, and a methylene group is still more preferable.

[0189] The structural unit represented by the formula (a4-4) is, for example, a methyl group corresponding to ^{R f21} in the structural unit (a4-4) in the following structural units and structural units represented by the following formulas: and a structural unit in which is substituted with a hydrogen atom.

[0190] When the resin (A) has the structural unit (a4), the content is preferably 1 to 20 mol%, more preferably 2 to 15 mol%, based on the total structural units of the resin (A). and 3-10 mol% is more preferable.

[0191] <Structural unit (a5)>

Examples of the non-leaving hydrocarbon group included in the structural unit (a5) include groups having a linear, branched or cyclic hydrocarbon group. Among them, the structural unit (a5) is preferably a group having an alicyclic hydrocarbon group.

Examples of the structural unit (a5) include a structural unit represented by the formula (a5-1).

[In formula (a5-1),

R ⁵¹ represents a hydrogen atom or a methyl group.

R ⁵² represents an alicyclic hydrocarbon group having 3 to 18 carbon atoms, and the hydrogen atom contained in the alicyclic hydrocarbon group may be substituted with an alicyclic hydrocarbon group having 1 to 8 carbon atoms.

L ⁵⁵ represents a single bond or a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O- or -CO-.]

[0192] ^{The alicyclic hydrocarbon group for R 52} may be either monocyclic or polycyclic. Examples of the monocyclic alicyclic hydrocarbon group include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group and a cyclohexyl group. Examples of the polycyclic alicyclic hydrocarbon group include an adamantyl group and a norbornyl group.

The aliphatic hydrocarbon group having 1 to 8 carbon atoms includes, for example, a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, an octyl group and a 2-ethylhexyl group. of an alkyl group.

As an alicyclic hydrocarbon group which has a substituent, 3-methyladamantyl group etc. are mentioned.

R ⁵² is preferably an unsubstituted alicyclic hydrocarbon group having 3 to 18 carbon atoms, more preferably an adamantyl group, a norbornyl group or a cyclohexyl group.

^Examples of the divalent saturated hydrocarbon group for L 55 include a divalent chain saturated hydrocarbon group and a divalent alicyclic saturated hydrocarbon group, and preferably a divalent chain saturated hydrocarbon group.

Examples of the divalent chain saturated hydrocarbon group include alkanediyl groups such as methylene group, ethylene group, propanediyl group, butanediyl group and pentanediyl group.

The divalent alicyclic saturated hydrocarbon group may be either monocyclic or polycyclic. Examples of the monocyclic alicyclic saturated hydrocarbon group include cycloalkanediyl groups such as a cyclopentanediyl group and a cyclohexanediyl group. Examples of the polycyclic divalent alicyclic saturated hydrocarbon group include an adamantanediyl group and a norbornanediyl group.

[0193] As a _{group in which -CH 2} - contained in the divalent saturated hydrocarbon group represented by ^{L 55} is substituted with -O- or -CO-, for example, it is represented by formulas (L1-1) to (L1-4) losing can be lifted. In the following formula, * and ** each represent a bond, and * represents a bond with an oxygen atom.

In formula (L1-1),

X ^x1 represents *-O-CO- or *-CO-O- (* represents a bond with ^{L x1).}

L ^x1 represents a divalent aliphatic saturated hydrocarbon group having 1 to 16 carbon atoms.

L ^x2 represents a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 15 carbon atoms.

However, the total carbon number of ^{L x1} and L ^{x2 is 16 or less.}

In formula (L1-2),

L ^x3 represents a divalent aliphatic saturated hydrocarbon group having 1 to 17 carbon atoms.

L ^x4 represents a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 16 carbon atoms.

However, the total carbon number of ^{L x3} and L ^{x4 is 17 or less.}

In formula (L1-3),

L ^x5 represents a divalent aliphatic saturated hydrocarbon group having 1 to 15 carbon atoms.

L ^x6 and L ^x7 each independently represent a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 14 carbon atoms.

However, the total number of carbon atoms of ^{L x5} , L ^x6 and L ^{x7 is 15 or less.}

In formula (L1-4),

L ^x8 and L ^x9 represent a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 12 carbon atoms.

W ^x1 represents a divalent alicyclic saturated hydrocarbon group having 3 to 15 carbon atoms.

However, the total number of carbon atoms of ^{L x8} , L ^x9 and W ^{x1 is 15 or less.}

[0194] L ^x1 is preferably a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a methylene group or an ethylene group.

L ^x2 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a single bond.

L ^x3 is preferably a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^x4 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^x5 is preferably a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a methylene group or an ethylene group.

L ^x6 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a methylene group or an ethylene group.

L ^x7 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms.

L ^x8 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a single bond or a methylene group.

L ^x9 is preferably a single bond or a divalent aliphatic saturated hydrocarbon group having 1 to 8 carbon atoms, more preferably a single bond or a methylene group.

W ^x1 is preferably a divalent alicyclic saturated hydrocarbon group having 3 to 10 carbon atoms, more preferably a cyclohexanediyl group or an adamantanediyl group.

[0195] Examples of the group represented by the formula (L1-1) include the following divalent groups.

[0196]

[0197] Examples of the group represented by the formula (L1-2) include the following divalent groups.

[0198] Examples of the group represented by the formula (L1-3) include the following divalent groups.

[0199] Examples of the group represented by the formula (L1-4) include the following divalent groups.

[0200] L ⁵⁵ is preferably a single bond or a group represented by formula (L1-1).

[0201] Examples of the structural unit (a5-1) include the structural units shown below and structural units in ^{which the methyl group corresponding to R 51} in the structural unit (a5-1) in the following structural units is substituted with a hydrogen atom.

[0202]

When resin (A) has a structural unit (a5), 1-30 mol% is preferable with respect to all the structural units of resin (A), and, as for the content rate, 2-20 mol% is more preferable, 3 ~15 mol% is more preferred.

[0203] <Structural unit (a6)>

Structural unit (a6) is a structural unit which has -SO ₂ - group, and _{it is preferable to have -SO 2} - group in a side chain.

-SO ₂ - is a structural unit having a group, -SO ₂ - may have a linear structure and having a group, -SO ₂ -, and optionally has a branch-like structure having a group, -SO ₂ - having an annular structure (monocyclic and polycyclic structure). Preferably, it is a _{structural unit which has a cyclic structure which has -SO 2} - group, More preferably, it is a structural unit which has a cyclic structure (sultone ring) containing _{-SO 2 -O-.}

Examples of the sultone ring include rings represented by the following formulas (T ^1-1 ), (T ^1-2 ), (T ^1-3 ) and (T ^1-4 ). The binding site may be in any position. Although monocyclic may be sufficient as a sultone ring, it is preferable that it is polycyclic. The sultone ring of the cyclic is, as the atomic group (原子團) constituting the ring, and means a cross-linked ring containing -SO ₂ -O-, formula (T ¹ -1) and the expression (T ¹ -2) shown by ring can be taken. The sultone ring may further contain a hetero atom other than _{-SO 2} -O- as an atomic group constituting the ring, like the ring represented by ^{formula (T 1-2).} As a hetero atom, an oxygen atom, a sulfur atom, or a nitrogen atom is mentioned, Preferably it is an oxygen atom.

[0205] The sultone ring may have a substituent, and as the substituent, an alkyl group having 1 to 12 carbon atoms, a halogen atom, a hydroxy group, a cyano group, an alkoxy group having 1 to 12 carbon atoms, and 6 to 12 carbon atoms, which may have a halogen atom or a hydroxy group Phosphorus aryl group, C7-12 aralkyl group, glycidyloxy group, C2-C12 alkoxycarbonyl group, C2-C4 alkylcarbonyl group, etc. are mentioned.

[0206] Examples of the halogen atom include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, a butyl group, a pentyl group, a hexyl group, an octyl group and a decyl group, preferably an alkyl group having 1 to 6 carbon atoms, and more preferably a methyl group.

Examples of the alkyl group having a halogen atom include a trifluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluoroisopropyl group, a perfluorobutyl group, a perfluorosec-butyl group, and a perfluorotert-butyl group. group, a perfluoropentyl group, a perfluorohexyl group, a trichloromethyl group, a tribromomethyl group and a triiodomethyl group, and preferably a trifluoromethyl group.

As an alkyl group which has a hydroxyl group, the hydroxyalkyl group of a hydroxymethyl group and 2-hydroxyethyl group is mentioned.

Examples of the alkoxy group include a methoxy group, an ethoxy group, a propoxy group, a butoxy group, a pentyloxy group, a hexyloxy group, a heptyloxy group, an octyloxy group, a decyloxy group, and a dodecyloxy group.

Examples of the aryl group include a phenyl group, a naphthyl group, an anthryl group, a p-methylphenyl group, a p-tert-butylphenyl group, a p-adamantylphenyl group, a tolyl group, a xylyl group, a cumyl group, a mesityl group, a biphenyl group, and a phenanthryl group. group, a 2,6-diethylphenyl group, and a 2-methyl-6-ethylphenyl group.

Examples of the aralkyl group include a benzyl group, a phenethyl group, a phenylpropyl group, a naphthylmethyl group, and a naphthylethyl group.

Examples of the alkoxycarbonyl group include a group in which an alkoxy group such as a methoxycarbonyl group and an ethoxycarbonyl group and a carbonyl group are bonded, preferably an alkoxycarbonyl group having 6 or less carbon atoms, and more preferably a methoxycarbonyl group.

Examples of the alkylcarbonyl group include an acetyl group, a propionyl group and a butyryl group.

[0207] From the viewpoint of facilitating the preparation of the monomer deriving the structural unit (a6), a sultone ring having no substituent is preferable.

As the sultone ring, a ring represented by the following formula (T1') is preferable.

[In formula (T1'),

X ¹¹ represents an oxygen atom, a sulfur atom, or a methylene group.

R ⁴¹ is an alkyl group having 1 to 12 carbon atoms, a halogen atom, a hydroxy group, a cyano group, an alkoxy group having 1 to 12 carbon atoms, an aryl group having 6 to 12 carbon atoms, or an aralkyl group having 7 to 12 carbon atoms which may have a halogen atom or a hydroxyl group , a glycidyloxy group, an alkoxycarbonyl group having 2 to 12 carbon atoms, or an alkylcarbonyl group having 2 to 4 carbon atoms.

ma represents the integer in any one of 0-9. When ma is 2 or more, a plurality of R ⁴¹ may be the same or different.

The binding site is any position.]

X ¹¹ is preferably an oxygen atom or a methylene group, more preferably a methylene group.

Examples of R ⁴¹ include the same substituents as the substituents of the sultone ring, and an alkyl group having 1 to 12 carbon atoms which may have a halogen atom or a hydroxy group is preferable.

[0208] As the sultone ring, the ring represented by the formula (T1) is more preferable.

[In formula (T1),

R ⁸ is an alkyl group having 1 to 12 carbon atoms, a halogen atom, a hydroxy group, a cyano group, an alkoxy group having 1 to 12 carbon atoms, an aryl group having 6 to 12 carbon atoms, or an aralkyl group having 7 to 12 carbon atoms which may have a halogen atom or a hydroxy group , a glycidyloxy group, an alkoxycarbonyl group having 2 to 12 carbon atoms, or an alkylcarbonyl group having 2 to 4 carbon atoms.

m represents the integer in any one of 0-9. When m is 2 or more, a plurality of R ⁸ may be the same or different.

The binding site is any position.]

[0209] Examples of R ⁸ include the same as those of ^{R 41 .}

ma in the formula (T1') and m in the formula (T1) are preferably 0 or 1, more preferably 0.

[0210] Examples of the ring represented by the formula (T1') and the ring represented by the formula (T1) include the following rings. The binding site is any position.

[0211] The structural unit having a sultone ring preferably has the following group. * in the following groups represents a binding site.

[0212] The _{structural unit having a -SO 2} - group preferably further has a group derived from a polymerizable group. Examples of the polymerizable group include a vinyl group, an acryloyl group, a methacryloyl group, an acryloyloxy group, a methacryloyloxy group, an acryloylamino group, a methacryloylamino group, an acryloylthio group, a methacryloylthio group, and the like. can be heard

Especially, the monomer which induces a structural unit (a6) becomes like this. Preferably it is a monomer which has an ethylenically unsaturated bond, More preferably, it is a (meth)acrylic-type monomer.

[0213] The structural unit (a6) is preferably a structural unit represented by formula (Ix).

[In formula (Ix), R ^x represents an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, a hydrogen atom, or a halogen atom.

A ^xx represents an oxygen atom, -N(R ^c )-, or a sulfur atom.

A ^x represents a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O-, -CO- or -N(R ^{d )-.}

X ¹¹ represents an oxygen atom, a sulfur atom, or a methylene group.

R ⁴¹ is an alkyl group having 1 to 12 carbon atoms, a halogen atom, a hydroxy group, a cyano group, an alkoxy group having 1 to 12 carbon atoms, an aryl group having 6 to 12 carbon atoms, or an aralkyl group having 7 to 12 carbon atoms which may have a halogen atom or a hydroxyl group , a glycidyloxy group, an alkoxycarbonyl group having 2 to 12 carbon atoms, or an alkylcarbonyl group having 2 to 4 carbon atoms.

ma represents the integer in any one of 0-9. When ma is 2 or more, a plurality of R ⁴¹ may be the same or different.

R ^c and R ^d each independently represent a hydrogen atom or an alkyl group having 1 to 6 carbon atoms.]

[0214] Examples ^{of the halogen atom for R x} include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

Examples of the alkyl group for R ^x include methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tert-butyl group, n-pentyl group and n-hexyl group. , Preferably it is a C1-C4 alkyl group, More preferably, it is a methyl group or an ethyl group.

Examples of the alkyl group having a halogen atom for R ^x include trifluoromethyl group, perfluoroethyl group, perfluoropropyl group, perfluoroisopropyl group, perfluorobutyl group, perfluorosec-butyl group, purple Luorotert-butyl group, perfluoropentyl group, perfluorohexyl group, trichloromethyl group, tribromomethyl group, triiodomethyl group, etc. are mentioned.

R ^x is preferably a hydrogen atom or an alkyl group having 1 to 4 carbon atoms, more preferably a hydrogen atom, a methyl group or an ethyl group, still more preferably a hydrogen atom or a methyl group.

[0215] Examples ^{of the divalent saturated hydrocarbon group of A x} include a linear alkanediyl group, a branched alkanediyl group, a monocyclic or polycyclic divalent alicyclic saturated hydrocarbon group, and combinations of two or more of these groups it may be one

Specifically, methylene group, ethylene group, propane-1,3-diyl group, propane-1,2-diyl group, butane-1,4-diyl group, pentane-1,5-diyl group, hexane-1, 6-diyl group, heptane-1,7-diyl group, octane-1,8-diyl group, nonane-1,9-diyl group, decane-1,10-diyl group, undecane-1,11-diyl group , dodecane-1,12-diyl group, tridecane-1,13-diyl group, tetradecane-1,14-diyl group, pentadecane-1,15-diyl group, hexadecane-1,16-diyl group straight-chain alkanediyl groups such as heptadecane-1,17-diyl group, ethane-1,1-diyl group, propane-1,1-diyl group and propane-2,2-diyl group;

Butane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group, 2-methylbutane-1,4 - branched alkanediyl groups, such as a diyl group;

Monocyclic 2, which is a cycloalkanediyl group, such as a cyclobutane-1,3-diyl group, a cyclopentane-1,3-diyl group, a cyclohexane-1,4-diyl group, and a cyclooctane-1,5-diyl group a valent alicyclic saturated hydrocarbon group;

Polycyclic divalent alicyclics, such as norbornane-1,4-diyl group, norbornane-2,5-diyl group, adamantane-1,5-diyl group, and adamantane-2,6-diyl group A saturated hydrocarbon group etc. are mentioned.

[0216] Examples of R ⁴¹ , X ¹¹ and ma include the same ones as in Formula (T1').

Examples of the sultone ring include those described above, and among them, the ones in which the bonding position is specified are preferable.

[0217] Examples of the structural unit (a6) include the following structural units.

[0218] Among them, formula (a6-1), formula (a6-2), formula (a6-6), formula (a6-7), formula (a6-8) and formula (a6-12) A structural unit is preferable, and the structural unit represented by a formula (a6-1), a formula (a6-2), a formula (a6-7), and (a6-8) is more preferable.

When resin (A) has a structural unit (a6), 1-50 mol% is preferable with respect to all the structural units of resin (A), and, as for the content rate, 2-40 mol% is more preferable, 3 ~30 mol% is more preferred.

[0219] <Structural unit (II)>

The resin (A) may further contain a structural unit (hereinafter, sometimes referred to as "structural unit (II)") which decomposes upon exposure to generate an acid. Specific examples of the structural unit (II) include the structural units described in Japanese Patent Application Laid-Open No. 2016-79235, and a structural unit having a sulfonate group or a carboxylate group in a side chain or an organic cation, or a sulfonio group in the side chain and a structural unit having an organic anion.

[0220] The structural unit having a sulfonate group or a carboxylate group and an organic cation in the side chain is preferably a structural unit represented by formula (II-2-A').

[Formula (II-2-A'),

X ^III3 represents a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O-, -S- or -CO-, and is included in the saturated hydrocarbon group The hydrogen atom to be used may be substituted with a halogen atom, an alkyl group having 1 to 6 carbon atoms which may have a halogen atom, or a hydroxy group.

A ^x1 represents a C1-C8 alkanediyl group, and the hydrogen atom contained in this alkanediyl group may be substituted by the fluorine atom or a C1-C6 perfluoroalkyl group.

RA ^- represents a sulfonate group or a carboxylate group.

R ^III3 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.

ZA ⁺ represents an organic cation.]

[0221] ^Examples of the halogen atom represented by R III3 include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by R ^III3 include the same groups as the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by ^{R a8 .}

Examples of the alkanediyl group having 1 to 8 carbon atoms represented by A ^x1 include a methylene group, an ethylene group, a propane-1,3-diyl group, a butane-1,4-diyl group, a pentane-1,5-diyl group, and a hexane- 1,6-diyl group, ethane-1,1-diyl group, propane-1,1-diyl group, propane-1,2-diyl group, propane-2,2-diyl group, pentane-2,4-di diyl, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group, 2-methylbutane-1,4-diyl group, and the like. have.

Examples of the optionally substituted perfluoroalkyl group having 1 to 6 carbon atoms for A ^x1 include a trifluoromethyl group, a perfluoroethyl group, a perfluoropropyl group, a perfluoroisopropyl group, a perfluorobutyl group, and a perfluoro and a losec-butyl group, a perfluorotert-butyl group, a perfluoropentyl group, and a perfluorohexyl group.

^Examples of the divalent saturated hydrocarbon group having 1 to 18 carbon atoms represented by X III3 include a linear or branched alkanediyl group and a monocyclic or polycyclic divalent alicyclic saturated hydrocarbon group, and combinations thereof may be used.

Specifically, methylene group, ethylene group, propane-1,3-diyl group, propane-1,2-diyl group, butane-1,4-diyl group, pentane-1,5-diyl group, hexane-1, 6-diyl group, heptane-1,7-diyl group, octane-1,8-diyl group, nonane-1,9-diyl group, decane-1,10-diyl group, undecane-1,11-diyl group , straight-chain alkanediyl groups such as dodecane-1,12-diyl groups; Butane-1,3-diyl group, 2-methylpropane-1,3-diyl group, 2-methylpropane-1,2-diyl group, pentane-1,4-diyl group, 2-methylbutane-1,4 - branched alkanediyl groups, such as a diyl group; cycloalkanediyl groups such as cyclobutane-1,3-diyl group, cyclopentane-1,3-diyl group, cyclohexane-1,4-diyl group and cyclooctane-1,5-diyl group; Divalent polycyclic alicyclic saturated groups such as norbornane-1,4-diyl group, norbornane-2,5-diyl group, adamantane-1,5-diyl group, and adamantane-2,6-diyl group A hydrocarbon group etc. are mentioned.

_{Examples of the -CH 2} - contained in the saturated hydrocarbon group substituted with -O-, -S- or -CO- include divalent groups represented by formulas (X1) to (X53). _{However, the number of carbon atoms before -CH 2} - contained in the saturated hydrocarbon group is substituted with -O-, -S- or -CO- is 17 or less, respectively. In the following formula, * and ** represent a binding site, and * represents a bond with ^{A x1.}

[0222] X ³ represents a divalent saturated hydrocarbon group having 1 to 16 carbon atoms.

X ⁴ represents a divalent saturated hydrocarbon group having 1 to 15 carbon atoms.

X ⁵ represents a divalent saturated hydrocarbon group having 1 to 13 carbon atoms.

X ⁶ represents a divalent saturated hydrocarbon group having 1 to 14 carbon atoms.

X ⁷ represents a trivalent saturated hydrocarbon group having 1 to 14 carbon atoms.

X ⁸ represents a divalent saturated hydrocarbon group having 1 to 13 carbon atoms.

^{[0223] ZA +} in the formula (II-2-A') includes the same ones as ^{the cation Z1 +} in the salt represented by the formula (B1).

[0224] The structural unit represented by the formula (II-2-A') is preferably a structural unit represented by the formula (II-2-A).

[In formula (II-2-A),

R ^III3 , X ^III3 and ZA ⁺ have the same meanings as above.

z2A represents the integer in any one of 0-6.

R ^III2 and R ^III4 each independently represent a hydrogen atom, a fluorine atom, or a perfluoroalkyl group having 1 to 6 carbon atoms, and when z2A is 2 or more, a plurality of R ^III2 and R ^III4 may be the same as or different from each other do.

Q ^a and Q ^b each independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.]

Examples of the perfluoroalkyl group having 1 to 6 carbon atoms represented by R ^III2 , R ^III4 , Q ^a and Q ^b include the same ones as the above-mentioned perfluoroalkyl group having 1 to 6 carbon atoms represented ^{by Q b1 .}

[0225] The structural unit represented by the formula (II-2-A) is preferably a structural unit represented by the formula (II-2-A-1).

[In formula (II-2-A-1),

R ^III2 , R ^III3 , R ^III4 , Q ^a , Q ^b and ZA ⁺ have the same meanings as above.

R ^III5 represents a saturated hydrocarbon group having 1 to 12 carbon atoms.

z2A1 represents the integer in any one of 0-6.

X ^I2 represents a divalent saturated hydrocarbon group having 1 to 11 carbon atoms, -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O-, -S- or -CO-, and is included in the saturated hydrocarbon group The hydrogen atom to be formed may be substituted with a halogen atom or a hydroxyl group.]

Examples of the saturated hydrocarbon group having 1 to 12 carbon atoms represented by R ^III5 include a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group, a sec-butyl group, a tert-butyl group, a pentyl group, a hexyl group, a heptyl group, and an octyl group. , a straight-chain or branched alkyl group such as a nonyl group, a decyl group, an undecyl group and a dodecyl group.

^Examples of the divalent saturated hydrocarbon group represented by X ^I2 include the same divalent saturated hydrocarbon group represented by X III3.

[0226] As the structural unit represented by the formula (II-2-A-1), the structural unit represented by the formula (II-2-A-2) is more preferable.

[In formula (II-2-A-2),

R ^III3 , R ^III5 and ZA ⁺ have the same meanings as above.

m and nA, independently of each other, represent 1 or 2.]

[0227] As the structural unit represented by the formula (II-2-A'), for example, the following structural unit, ^{a group corresponding to the methyl group of R III3} has a hydrogen atom, a halogen atom (eg, a fluorine atom) or a halogen atom The structural unit substituted with the optionally C1-C6 alkyl group (for example, trifluoromethyl group, etc.) and the structural unit of International Publication No. 2012/050015 are mentioned. ZA ⁺ represents an organic cation.

[0228] The structural unit having a sulfonio group and an organic anion in the side chain is preferably a structural unit represented by formula (II-1-1).

[In formula (II-1-1),

A ^II1 represents a single bond or a divalent linking group.

R ^II1 represents a divalent aromatic hydrocarbon group having 6 to 18 carbon atoms.

R ^II2 and R ^II3 each independently represent a hydrocarbon group having 1 to 18 carbon atoms, and R ^II2 and R ^II3 may be bonded to each other to form a ring together with the sulfur atom to which they are bonded.

R ^II4 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.

A ^- represents an organic anion.]

Examples of the divalent aromatic hydrocarbon group having 6 to 18 carbon atoms represented by R ^{II1 include a phenylene group and a naphthylene group.}

^Examples of the hydrocarbon group represented by R ^II2 and R II3 include an alkyl group, an alicyclic hydrocarbon group, an aromatic hydrocarbon group, and a group formed by combining these groups.

^Examples of the halogen atom represented by R II4 include a fluorine atom, a chlorine atom, a bromine atom and an iodine atom.

Examples of the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by R ^II4 include the same groups as the alkyl group having 1 to 6 carbon atoms which may have a halogen atom represented by ^{R a8 .}

Examples of the divalent linking group represented by A ^II1 include a divalent saturated hydrocarbon group having 1 to 18 carbon atoms, and -CH ₂ - contained in the divalent saturated hydrocarbon group is -O-, -S- or -CO - may be substituted. Specific examples include the same divalent saturated hydrocarbon group having 1 to 18 carbon atoms represented by ^{X III3.}

[0229] As the structural unit containing a cation in the formula (II-1-1), the structural unit shown below and ^{a group corresponding to the methyl group of R II4} are substituted with a hydrogen atom, a fluorine atom, a trifluoromethyl group, etc. structural units; and the like.

[0230] ^{Examples of the organic anion represented by A −} include a sulfonic acid anion, a sulfonylimide anion, a sulfonylmethide anion, and a carboxylate anion. A ^{sulfonic acid anion is preferable and, as for the organic anion represented by A -} , as a sulfonic acid anion, it is more preferable that it is an anion contained in the salt represented by Formula (B1) mentioned above. Sulfonyl imide anion, a sulfonate anion and nilme suited carboxylic acid anion is the anion AI contained in the salt represented by the aforementioned formula (I) ^- are more preferable in that.

[0231] Examples of the structural unit represented by the formula (II-1-1) include the structural units shown below.

[0232] In the case of containing the structural unit (II) in the resin (A), the content of the structural unit (II) is preferably 1 to 20 mol% with respect to the total structural units of the resin (A), more Preferably it is 2-15 mol%, More preferably, it is 3-10 mol%.

[0233] The resin (A) may have structural units other than the structural units described above, and examples of such structural units include structural units well-known in the art.

[0234] The resin (A) is preferably a resin composed of the structural unit (a1) and the structural unit (s), that is, a copolymer of the monomer (a1) and the monomer (s).

The structural unit (a1) is preferably a structural unit (a1-0), a structural unit (a1-1) and a structural unit (a1-2) (preferably the structural unit having a cyclohexyl group and a cyclopentyl group) at least one selected from the group consisting of, more preferably at least two, still more preferably at least two selected from the group consisting of a structural unit (a1-1) and a structural unit (a1-2). .

The structural unit (s) is preferably at least one selected from the group consisting of the structural unit (a2) and the structural unit (a3). The structural unit (a2) is preferably a structural unit (a2-1) or a structural unit (a2-A). The structural unit (a3) is preferably selected from the group consisting of a structural unit represented by formula (a3-1), a structural unit represented by formula (a3-2), and a structural unit represented by formula (a3-4) There is at least one

Each structural unit constituting the resin (A) may be used alone or in combination of two or more, and may be prepared by a known polymerization method (eg, radical polymerization method) using a monomer that induces these structural units. can The content rate of each structural unit which resin (A) has can be adjusted by the usage-amount of the monomer used for superposition|polymerization.

The weight average molecular weight of the resin (A) is preferably 2,000 or more (more preferably 2,500 or more, still more preferably 3,000 or more), and 50,000 or less (more preferably 30,000 or less, still more preferably 15,000 or less). . In the present specification, the weight average molecular weight is a value obtained under the conditions described in Examples by gel permeation chromatography.

[0235] <Resin other than Resin (A)>

In the resist composition of the present invention, a resin other than the resin (A) may be used in combination.

Examples of the resin other than the resin (A) include resins containing the structural unit (a4) or the structural unit (a5) (hereinafter sometimes referred to as resin (X)).

Especially as resin (X), resin containing a structural unit (a4) is preferable.

In the resin (X), the content of the structural unit (a4) is preferably 30 mol% or more, more preferably 40 mol% or more, and 45 mol% or more, with respect to the total of all structural units of the resin (X). more preferably.

Examples of the structural unit that the resin (X) may further include a structural unit (a1), a structural unit (a2), a structural unit (a3), and a structural unit derived from other known monomers. Especially, it is preferable that resin (X) is resin which consists only of a structural unit (a4) and/or a structural unit (a5).

Each structural unit constituting the resin (X) may be used alone or in combination of two or more, and may be prepared by a known polymerization method (eg, radical polymerization method) using a monomer that induces these structural units. can The content rate of each structural unit which resin (X) has can be adjusted by the usage-amount of the monomer used for superposition|polymerization.

The weight average molecular weight of the resin (X) is preferably 6,000 or more (more preferably 7,000 or more) and 80,000 or less (more preferably 60,000 or less). The measuring means of the weight average molecular weight of resin (X) is the same as that in the case of resin (A).

[0236] When the resist composition of the present invention contains the resin (X), its content is preferably 1 to 60 parts by mass, more preferably 1 to 50 parts by mass, based on 100 parts by mass of the resin (A). It is a mass part, More preferably, it is 1-40 mass parts, More preferably, it is 1-30 mass parts, Especially preferably, it is 1-8 mass parts.

[0237] The content of the resin (A) in the resist composition is preferably 80% by mass or more and 99% by mass or less, and more preferably 90% by mass or more and 99% by mass or less, based on the solid content of the resist composition. do. Further, when a resin other than the resin (A) is included, the total content of the resin (A) and the resin other than the resin (A) is preferably 80% by mass or more and 99% by mass or less with respect to the solid content of the resist composition. , 90 mass % or more and 99 mass % or less are more preferable. In the present specification, "solid content of the resist composition" means the total amount of components obtained by subtracting the solvent (E) described later from the total amount of the resist composition. The solid content of the resist composition and the resin content thereof can be measured by known analytical means such as liquid chromatography or gas chromatography.

[0238] <Solvent (E)>

The content of the solvent (E) in the resist composition is usually 90% by mass or more and 99.9% by mass or less, preferably 92% by mass or more and 99% by mass or less, and more preferably 94% by mass or more and 99% by mass or less. The content of the solvent (E) can be measured, for example, by known analytical means such as liquid chromatography or gas chromatography.

[0239] Examples of the solvent (E) include glycol ether esters such as ethyl cellosolve acetate, methyl cellosolve acetate, and propylene glycol monomethyl ether acetate; glycol ethers such as propylene glycol monomethyl ether; esters such as ethyl lactate, butyl acetate, amyl acetate, and ethyl pyruvate; ketones such as acetone, methyl isobutyl ketone, 2-heptanone and cyclohexanone; cyclic esters such as γ-butyrolactone; and the like. One type of solvent (E) may be used independently and 2 or more types may be used for it.

[0240] ＜??wife (C)＞

Salts which generate an acid with weaker acidity than the acid which generate|occur|produce from a basic nitrogen-containing organic compound and an acid generator (B) are mentioned as a target (C). When the resist composition contains the material (C), the content of the material (C) is preferably about 0.01 to 15 mass%, and 0.01 to 10 mass%, based on the amount of solid content in the resist composition. It is more preferable that it is about 0.1-5 mass %, It is still more preferable that it is about 0.1-3 mass %.

Examples of the basic nitrogen-containing organic compound include amines and ammonium salts. Examples of the amine include aliphatic amines and aromatic amines. Examples of the aliphatic amine include a primary amine, a secondary amine, and a tertiary amine.

[0241] As the amine, 1-naphthylamine, 2-naphthylamine, aniline, diisopropylaniline, 2-, 3- or 4-methylaniline, 4-nitroaniline, N-methylaniline, N,N- Dimethylaniline, diphenylamine, hexylamine, heptylamine, octylamine, nonylamine, decylamine, dibutylamine, dipentylamine, dihexylamine, diheptylamine, dioctylamine, dinonylamine, didecylamine, Triethylamine, trimethylamine, tripropylamine, tributylamine, tripentylamine, trihexylamine, triheptylamine, trioctylamine, trinonylamine, tridecylamine, methyldibutylamine, methyldipentylamine, methyl Dihexylamine, methyldicyclohexylamine, methyldiheptylamine, methyldioctylamine, methyldinonylamine, methyldidecylamine, ethyldibutylamine, ethyldipentylamine, ethyldihexylamine, ethyldiheptylamine, Ethyldioctylamine, ethyldinonylamine, ethyl didecylamine, dicyclohexylmethylamine, tris[2-(2-methoxyethoxy)ethyl]amine, triisopropanolamine, ethylenediamine, tetramethylenediamine, hexamethylene Diamine, 4,4'-diamino-1,2-diphenylethane, 4,4'-diamino-3,3'-dimethyldiphenylmethane, 4,4'-diamino-3,3'-di Ethyldiphenylmethane, 2,2'-methylenebisaniline, imidazole, 4-methylimidazole, pyridine, 4-methylpyridine, 1,2-di(2-pyridyl)ethane, 1,2-di( 4-pyridyl)ethane, 1,2-di(2-pyridyl)ethene, 1,2-di(4-pyridyl)ethene, 1,3-di(4-pyridyl)propane, 1,2- Di(4-pyridyloxy)ethane, di(2-pyridyl)ketone, 4,4'-dipyridylsulfide, 4,4'-dipyridyldisulfide, 2,2'-dipyridylamine, 2,2'-dipicolylamine, bipyridine, etc. are mentioned, Preferably diisopropylaniline is mentioned, More preferably, 2,6-diisopropylaniline is mentioned.

[0242] As the ammonium salt, tetramethylammonium hydroxide, tetraisopropylammonium hydroxide, tetrabutylammonium hydroxide, tetrahexylammonium hydroxide, tetraoctylammonium hydroxide, phenyltrimethylammonium hydroxide, 3 -(trifluoromethyl)phenyltrimethylammonium hydroxide, tetra-n-butylammonium salicylate, choline, etc. are mentioned.

[0243] The acidity of the salt that generates an acid having a weaker acidity than the acid generated from the acid generator (B) is expressed by the acid dissociation constant (pKa). The salt that generates an acid having a weaker acidity than the acid generated from the acid generator (B) is a salt in which the acid dissociation constant of the acid generated from the salt is usually -3 < pKa, preferably -1 < pKa < It is a salt of 7, More preferably, it is a salt of 0<pKa<5.

Examples of the salt that generates an acid having a weaker acidity than the acid generated from the acid generator (B) include a salt represented by the following formula, and a salt represented by the formula (D) described in Japanese Patent Application Laid-Open No. 2015-147926 (hereinafter, "Weak acid intramolecular salt (D)."), and Japanese Patent Laid-Open No. 2012-229206, Japanese Patent Application Laid-Open No. 2012-6908, Japanese Patent Application Laid-Open No. 2012-72109, Japanese Patent The salts of Unexamined-Japanese-Patent No. 2011-39502 and Unexamined-Japanese-Patent No. 2011-191745 are mentioned. The salt for generating an acid having a weaker acidity than the acid generated from the acid generator (B) is preferably a salt for generating a carboxylic acid having a weaker acidity than the acid generated from the acid generator (B) (carboxylic acid) salt having an anion), and more preferably, a weak acid intramolecular salt (D).

[0244] Examples of the weak acid intramolecular salt (D) include the following salts.

[0245] <Other ingredients>

The resist composition of the present invention may contain components other than the above-mentioned components (hereinafter sometimes referred to as &quot;other components (F)&quot;) as needed. The other component (F) is not particularly limited, and additives known in the resist field, for example, a sensitizer, a dissolution inhibitor, a surfactant, a stabilizer, a dye, and the like can be used.

[0246] <Preparation of resist composition>

The resist composition of the present invention comprises a salt (I), a resin (A) and an acid generator (B), and, if necessary, a resin other than the resin (A) used, a solvent (E), and a solvent (C). ) and other components (F) can be mixed. The mixing order is arbitrary and is not particularly limited. The temperature at the time of mixing is 10-40 degreeC, and suitable temperature can be selected according to the kind of resin, etc., the solubility with respect to the solvent (E), etc. of resin. As for the mixing time, an appropriate time can be selected from 0.5 to 24 hours according to the mixing temperature. In addition, there is no restriction|limiting in particular also in a mixing means, A stirring mixing etc. can be used.

After mixing each component, it is preferable to filter using the filter with a pore diameter of about 0.003-0.2 micrometer.

[0247] <Method for producing resist pattern>

The method for producing a resist pattern of the present invention comprises:

(1) a step of applying the resist composition of the present invention on a substrate;

(2) drying the composition after application to form a composition layer;

(3) a step of exposing the composition layer;

(4) heating the composition layer after exposure, and

(5) The process of developing the composition layer after heating is included.

In order to apply a resist composition on a substrate, it is possible to carry out with a commonly used apparatus, such as a spin coater. Examples of the substrate include inorganic substrates such as silicon wafers. Before apply|coating a resist composition, a board|substrate may be wash|cleaned, and the antireflection film etc. may be formed on the board|substrate.

By drying the composition after application|coating, a solvent is removed and a composition layer is formed. Drying is performed, for example by evaporating a solvent using heating apparatuses, such as a hotplate (so-called pre-bake), or using a pressure reducing apparatus. It is preferable that heating temperature is 50-200 degreeC, and, as for heating time, it is preferable that it is 10-180 second. Moreover, it is preferable that the pressure at the time of drying under reduced pressure is ^{about 1-1.0x10 5 Pa.}

The obtained composition layer is exposed using an exposure machine normally. The exposure machine may be an immersion exposure machine. Examples of the exposure light source include those emitting laser light in the ultraviolet region such as KrF excimer laser (wavelength 248 nm), ArF excimer laser (wavelength 193 nm), and F ₂ excimer laser (wavelength 157 nm), and solid-state laser light source (YAG or semiconductor laser, etc.) It is possible to use a variety of methods, such as converting a laser beam from a wavelength to irradiating a harmonic laser beam in the far-ultraviolet region or vacuum ultraviolet region, or irradiating an electron beam or ultra-ultraviolet light (EUV). In addition, in this specification, irradiating these radiations may be generically called "exposure". At the time of exposure, exposure is normally performed through the mask corresponding to the requested|required pattern. When an exposure light source is an electron beam, you may expose by drawing directly, without using a mask.

The composition layer after exposure is subjected to heat treatment (so-called post exposure bake (PEB)) in order to accelerate the deprotection reaction in the acid labile group. Heating temperature is about 50-200 degreeC normally, Preferably it is about 70-150 degreeC.

The composition layer after heating is usually developed using a developing solution using a developing device. As a developing method, the dipping method, the puddle method, the spray method, the dynamic dispensing method, etc. are mentioned. It is preferable that image development temperature is 5-60 degreeC, for example, and it is preferable that image development time is 5-300 second, for example. A positive type resist pattern or a negative type resist pattern can be manufactured by selecting the kind of developing solution as follows.

When producing a positive resist pattern from the resist composition of the present invention, an alkaline developer is used as the developer. The alkaline developer may be various alkaline aqueous solutions used in this field. For example, the aqueous solution of tetramethylammonium hydroxide and (2-hydroxyethyl) trimethylammonium hydroxide (common name choline), etc. are mentioned. The alkali developer may contain surfactant.

It is preferable to wash the resist pattern after development with ultrapure water, and then to remove the water remaining on the substrate and the pattern.

When producing a negative resist pattern from the resist composition of the present invention, a developer containing an organic solvent (hereinafter, sometimes referred to as an "organic developer") is used as the developer.

Examples of the organic solvent contained in the organic developer include ketone solvents such as 2-hexanone and 2-heptanone; glycol ether ester solvents such as propylene glycol monomethyl ether acetate; ester solvents such as butyl acetate; glycol ether solvents such as propylene glycol monomethyl ether; amide solvents such as N,N-dimethylacetamide; Aromatic hydrocarbon solvents, such as anisole, etc. are mentioned.

In the organic developer, the content of the organic solvent is preferably 90% by mass or more and 100% by mass or less, more preferably 95% by mass or more and 100% by mass or less, and still more preferably only an organic solvent.

Especially, as an organic type developing solution, the developing solution containing butyl acetate and/or 2-heptanone is preferable. In the organic developer, the total content of butyl acetate and 2-heptanone is preferably 50% by mass or more and 100% by mass or less, more preferably 90% by mass or more and 100% by mass or less, and substantially butyl acetate and/or 2-heptanone More preferably, it is only heptanone.

The organic developer may contain a surfactant. In addition, a trace amount of water may be contained in the organic developer.

During development, the development may be stopped by substituting with a solvent different from that of the organic developer.

It is preferable to wash the resist pattern after development with a rinse solution. The rinse liquid is not particularly limited as long as it does not dissolve the resist pattern, and a solution containing a general organic solvent can be used, and an alcohol solvent or an ester solvent is preferable.

After cleaning, it is preferable to remove the rinse liquid remaining on the substrate and the pattern.

[0248] <Use>

The resist composition of the present invention is a resist composition for KrF excimer laser exposure, a resist composition for ArF excimer laser exposure, a resist composition for electron beam (EB) exposure, or a resist composition for EUV exposure, particularly a resist composition for electron beam (EB) exposure, or a resist composition for EUV exposure It is suitable as a resist composition of

[Example]

[0249] By way of Examples, the present invention will be described in more detail. In the examples, "%" and "part" indicating the content or the amount used are based on mass unless otherwise specified.

A weight average molecular weight is the value calculated|required by gel permeation chromatography. In addition, the analysis conditions of the gel permeation chromatography are as follows.

Column: TSKgel Multipore HXL-M x 3+guardcolumn (manufactured by TOSOH CORPORATION)

Eluent: tetrahydrofuran

Flow rate: 1.0 mL/min

Detector: RI Detector

Column temperature: 40°C

Injection volume: 100μl

Molecular weight standard: standard polystyrene (manufactured by TOSOH CORPORATION)

The structure of the compound was confirmed by measuring molecular ion peaks using mass spectrometry (LC: 1100 manufactured by Agilent, MASS is LC/MSD manufactured by Agilent). In the following examples, the value of this molecular ion peak is expressed as "MASS".

[0250] Example 1: Synthesis of salt represented by formula (I-915)

20 parts of the compound represented by the formula (I-915-a), 2.28 parts of the compound represented by the formula (I-915-c), 100 parts of ethyl acetate and 15 parts of tetrahydrofuran were mixed, followed by stirring at 23° C. for 30 minutes. . To the resulting mixed solution, 6.55 parts of a compound represented by the formula (I-915-b) was added, and the mixture was stirred at 23°C for 18 hours. To the obtained reaction mass, 20 parts of n-heptane and 70 parts of ion-exchanged water were added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. After adding 60 parts of ion-exchanged water to the recovered organic layer and stirring at 23° C. for 30 minutes, the organic layer was separated by separation. This water washing operation was repeated 4 times. The obtained organic layer was concentrated, and the concentrated mass was column (silica gel 60N (spherical, neutral) 100-210 µm; manufactured by Kanto Chemical Co., Inc., developing solvent: n-heptane/ethyl acetate = 1/1) By fractionation, 7.48 parts of a compound represented by the formula (I-915-d) was obtained.

0.95 parts of the compound represented by the formula (I-915-d) and 10 parts of tetrahydrofuran were mixed, stirred at 23°C for 30 minutes, cooled to 5°C, and 0.14 parts of sodium hydride was added. To the resulting mixture, 1.01 parts of a salt represented by the formula (I-915-e) was added, and stirred at 5° C. for 3 hours. To the obtained mixture, after adding 6.30 parts of 1N hydrochloric acid, the temperature was raised to 23° C. and stirred at 23° C. for 6 hours. To the obtained mixture, 30 parts of chloroform and 15 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. After concentrating the obtained organic layer, 1 part of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, and then the supernatant was removed and concentrated by formula (I- 1.24 parts of the salt represented by 915-f) were obtained.

0.99 parts of the salt represented by the formula (I-915-f), 0.80 parts of the salt represented by the formula (I-915-g) and 20 parts of chloroform were added, and the mixture was stirred at 23° C. for 3 hours. 15 parts of ion-exchanged water was added to the obtained reaction material, and after stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. After adding 15 parts of ion-exchanged water to the obtained organic layer, and stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 5 times. After concentrating the obtained organic layer, 1.5 parts of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, to formula (I-915) 1.31 parts of the indicated salt were obtained.

MASS(ESI(+) Spectrum):M ⁺ 497.0

MASS(ESI(-) Spectrum):M ^- 323.0

[0251] Example 2: Synthesis of salt represented by formula (I-920)

0.99 parts of the salt represented by the formula (I-915-f), 1.20 parts of the salt represented by the formula (I-920-g) and 20 parts of chloroform were added, and the mixture was stirred at 23° C. for 3 hours. 15 parts of ion-exchanged water was added to the obtained reaction material, and after stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. After adding 15 parts of ion-exchanged water to the obtained organic layer, and stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 5 times. After concentrating the obtained organic layer, 1.5 parts of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, to formula (I-920) 1.44 parts of the indicated salt were obtained.

MASS(ESI(+) Spectrum):M ⁺ 497.0

MASS(ESI(-) Spectrum):M ^- 517.1

[0252] Example 3: Synthesis of salt represented by formula (I-953)

0.62 parts of a salt represented by the formula (I-915-f) and 30 parts of dimethylformamide are mixed, stirred at 23°C for 30 minutes, 0.16 parts of potassium carbonate and 0.05 parts of potassium iodide are added, and the temperature is raised to 75°C did it To the resulting mixture, 1.13 parts of a compound represented by the formula (I-953-a) was added, stirred at 75°C for 5 hours, and then cooled to 23°C. To the obtained mixture, 50 parts of chloroform and 20 parts of a 5% aqueous oxalic acid solution were added, stirred at 23° C. for 30 minutes, and the mixture was separated and the organic layer was extracted. 20 parts of ion-exchanged water was added to the obtained organic layer, and after stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 5 times. By concentrating the obtained organic layer, 0.88 parts of a compound represented by Formula (I-953-b) was obtained.

0.76 parts of the salt represented by the formula (I-953-b), 0.34 parts of the salt represented by the formula (I-915-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, and to the concentration residue, 30 parts of tert-butylmethyl ether was added, stirred at 23°C for 30 minutes, and filtered to obtain 0.89 parts of a salt represented by the formula (I-953).

MASS(ESI(+) Spectrum):M ⁺ 909.3

MASS(ESI(-) Spectrum):M ^- 323.0

[0253] Example 4: Synthesis of salt represented by formula (I-958)

0.76 parts of the salt represented by the formula (I-953-b), 0.51 parts of the salt represented by the formula (I-920-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, and to the concentration residue, 30 parts of tert-butylmethyl ether was added, stirred at 23°C for 30 minutes, and then filtered to obtain 0.97 parts of a salt represented by the formula (I-958).

MASS(ESI(+) Spectrum):M ⁺ 909.3

MASS(ESI(-) Spectrum):M ^- 517.1

[0254] Example 5: Synthesis of salt represented by formula (I-966)

0.76 parts of the salt represented by the formula (I-963-b), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, and to the concentration residue, 30 parts of tert-butylmethyl ether was added, stirred at 23°C for 30 minutes, and then filtered to obtain 0.92 parts of a salt represented by the formula (I-966).

MASS(ESI(+) Spectrum):M ⁺ 909.3

MASS(ESI(-) Spectrum):M ^- 467.1

[0255] Example 6: Synthesis of salt represented by formula (I-236)

3.80 parts of the compound represented by the formula (I-236-a) and 6.40 parts of Oxone (registered trademark) were mixed, stirred at 23°C for 30 minutes, and then cooled to 5°C. After adding 23.56 parts of sulfuric acid to the obtained mixture, it stirred at 5 degreeC for 30 minute(s). To the resulting mixture, a mixed solution of 3.68 parts of the compound represented by the formula (I-236-b) and 18.40 parts of chloroform was added, stirred at 5°C for 30 minutes, and further stirred at 23°C for 2 hours. After adding the obtained mixed solution to 120 parts of methanol and stirring at 23 degreeC for 30 minute(s), it filtered. After concentrating the obtained filtrate, to the concentrated residue, 125 parts of chloroform and 25 parts of acetonitrile were added, stirred at 23° C. for 30 minutes, 60 parts of 5% hydrochloric acid was added and stirred at 23° C. for 30 minutes, followed by separation and an organic layer was extracted. After adding 40 parts of ion-exchanged water to the obtained organic layer and stirring at 23 degreeC for 30 minutes, it liquid-separated and the organic layer was extracted. This washing operation was repeated 3 times. The resulting organic layer was concentrated, and 45 parts of tert-butylmethyl ether was added to the concentrated mixture, stirred at 23°C for 30 minutes, and filtered to obtain 2.37 parts of a salt represented by the formula (I-236-c).

0.95 parts of the compound represented by the formula (I-915-d) and 10 parts of tetrahydrofuran were mixed, stirred at 23°C for 30 minutes, cooled to 5°C, and 0.14 parts of sodium hydride was added. To the resulting mixture, 2.32 parts of a salt represented by the formula (I-236-c) was added, and stirred at 5° C. for 3 hours. To the obtained mixture, after adding 6.30 parts of 1N hydrochloric acid, the temperature was raised to 23° C. and stirred at 23° C. for 6 hours. To the obtained mixture, 30 parts of chloroform and 15 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. After concentrating the obtained organic layer, 1 part of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, and the formula (I-236-f ) of the salt represented by 2.19 parts.

0.93 parts of the salt represented by the formula (I-236-f), 1.20 parts of the salt represented by the formula (I-920-g) and 20 parts of chloroform were added, and the mixture was stirred at 23° C. for 3 hours. 15 parts of ion-exchanged water was added to the obtained reaction material, and after stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. After adding 15 parts of ion-exchanged water to the obtained organic layer, and stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 5 times. After concentrating the obtained organic layer, 1.5 parts of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant solution was removed and concentrated, to formula (I-236) 1.52 parts of the indicated salt were obtained.

MASS(ESI(+) Spectrum):M ⁺ 459.1

MASS(ESI(-) Spectrum):M ^- 517.1

[0256] Example 7: Synthesis of salt represented by formula (I-274)

1.37 parts of the salt represented by the formula (I-236-f) and 30 parts of dimethylformamide are mixed, stirred at 23°C for 30 minutes, 0.16 parts of potassium carbonate and 0.05 parts of potassium iodide are added, and the temperature is raised to 75°C did it To the resulting mixture, 1.13 parts of a compound represented by the formula (I-953-a) was added, stirred at 75°C for 5 hours, and then cooled to 23°C. To the obtained mixture, 50 parts of chloroform and 20 parts of a 5% aqueous oxalic acid solution were added, stirred at 23° C. for 30 minutes, and the mixture was separated and the organic layer was extracted. 20 parts of ion-exchanged water was added to the obtained organic layer, and after stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 5 times. By concentrating the obtained organic layer, 1.55 parts of a compound represented by Formula (I-274-b) was obtained.

0.56 parts of the salt represented by the formula (I-274-b), 0.51 parts of the salt represented by the formula (I-920-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23°C for 30 minutes, and then filtered to obtain 0.71 parts of a salt represented by the formula (I-274).

MASS(ESI(+) Spectrum):M ⁺ 665.2

MASS(ESI(-) Spectrum):M ^- 517.1

[0257] Example 8: Synthesis of the salt represented by the formula (I-282)

0.56 parts of the salt represented by the formula (I-274-b), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The resulting organic layer was concentrated, and 30 parts of tert-butylmethyl ether was added to the concentrated residue, stirred at 23°C for 30 minutes, and filtered to obtain 0.68 parts of a salt represented by the formula (I-282).

MASS(ESI(+) Spectrum):M ⁺ 665.2

MASS(ESI(-) Spectrum):M ^- 467.1

[0258] Example 9: Synthesis of salt represented by formula (I-1764)

0.95 parts of the compound represented by the formula (I-915-d) and 10 parts of tetrahydrofuran were mixed, stirred at 23°C for 30 minutes, cooled to 5°C, and 0.14 parts of sodium hydride was added. To the resulting mixture, 1.01 parts of a salt represented by the formula (I-915-e) was added, and after stirring at 5°C for 3 hours, the temperature was raised to 23°C and stirred at 23°C for 1 hour. To the obtained mixture, 30 parts of chloroform and 15 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. After concentrating the obtained organic layer, 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, and the salt represented by the formula (I-1764-f) 1.52 copies were obtained.

0.54 parts of the salt represented by the formula (I-1764-b), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, and 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23°C for 30 minutes, and then filtered to obtain 0.71 parts of the salt represented by the formula (I-1764).

MASS(ESI(+) Spectrum):M ⁺ 641.1

MASS(ESI(-) Spectrum):M ^- 467.1

[0259] Example 10: Synthesis of the salt represented by the formula (I-1802)

10.12 parts of the compound represented by the formula (I-1802-d), 7.77 parts of the salt represented by the formula (I-915-e) and 90 parts of dimethylformamide are mixed, stirred at 23° C. for 30 minutes, and then heated to 90° C. The temperature was raised. To the resulting mixture, 14.41 parts of potassium carbonate was added, stirred at 90°C for 3 hours, and then cooled to 23°C. To the obtained mixture, 200 parts of chloroform and 150 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. To the obtained organic layer, 150 parts of ion-exchanged water was added, and after stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 3 times. After concentrating the obtained organic layer, 5 parts of acetonitrile and 150 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, and the formula (I-1802-f 13.12 parts of the salt represented by ) was obtained.

0.56 parts of the salt represented by the formula (I-1802-f), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, and 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23 degreeC for 30 minutes, and filtered, 0.81 part of salt represented by Formula (I-1802) was obtained.

MASS(ESI(+) Spectrum):M ⁺ 665.1

MASS(ESI(-) Spectrum):M ^- 467.1

[0260] Example 11: Synthesis of salt represented by formula (I-1460)

0.95 parts of the compound represented by the formula (I-915-d) and 10 parts of tetrahydrofuran were mixed, stirred at 23°C for 30 minutes, cooled to 5°C, and 0.14 parts of sodium hydride was added. To the obtained mixture, 2.32 parts of a salt represented by the formula (I-236-c) was added, and after stirring at 5°C for 3 hours, the temperature was raised to 23°C and stirred at 23°C for 1 hour. To the obtained mixture, 30 parts of chloroform and 15 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. After concentrating the obtained organic layer, 1 part of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, and the formula (I-1460-f ) of the salt represented by 2.74 parts.

0.45 parts of the salt represented by the formula (I-1460-f), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23°C for 30 minutes, and then filtered to obtain 0.62 parts of a salt represented by the formula (I-1460).

MASS(ESI(+) Spectrum):M ⁺ 531.1

MASS(ESI(-) Spectrum):M ^- 467.1

[0261] Example 12: Synthesis of the salt represented by the formula (I-1574)

1.01 parts of the compound represented by the formula (I-1802-d), 1.78 parts of the salt represented by the formula (I-236-e) and 20 parts of dimethylformamide are mixed, stirred at 23° C. for 30 minutes, and then heated to 90° C. The temperature was raised. To the resulting mixture, 1.44 parts of potassium carbonate was added, stirred at 90°C for 3 hours, and then cooled to 23°C. To the obtained mixture, 30 parts of chloroform and 15 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. After adding 15 parts of ion-exchanged water to the obtained organic layer, and stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 3 times. After concentrating the obtained organic layer, to the concentration residue, 1 part of acetonitrile and 30 parts of tert-butylmethyl ether were added, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, and the formula (I-1574-f ) of the salt represented by 1.99 parts.

0.46 parts of the salt represented by the formula (I-1574-f), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, and 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23 degreeC for 30 minutes, and filtered, 0.69 parts of salt represented by Formula (I-1574) was obtained.

MASS(ESI(+) Spectrum):M ⁺ 543.1

MASS(ESI(-) Spectrum):M ^- 467.1

[0262] Example 13: Synthesis of the salt represented by the formula (I-1536)

6.57 parts of the compound represented by the formula (I-1536-a), 0.23 parts of the compound represented by the formula (I-915-c), 30 parts of ethyl acetate and 15 parts of tetrahydrofuran were mixed, and stirred at 23° C. for 30 minutes. . To the resulting mixed solution, 0.66 parts of a compound represented by formula (I-915-b) was added, and the mixture was stirred at 23° C. for 18 hours. To the obtained reaction mass, 100 parts of n-heptane and 20 parts of ion-exchanged water were added, and after stirring at 23 degreeC for 30 minutes, it liquid-separated and the organic layer was extracted. 20 parts of ion-exchanged water was added to the recovered organic layer, and the mixture was stirred at 23° C. for 30 minutes, followed by separation to extract the organic layer. This washing operation was repeated 4 times. The obtained organic layer was concentrated, and the concentrated mass was separated by column (silica gel 60N (spherical, neutral) 100-210 µm; manufactured by Kanto Chemical Co., Inc., developing solvent: n-heptane/ethyl acetate = 1/1), 6.28 parts of the compound represented by (I-1536-d) was obtained.

2.26 parts of the compound represented by the formula (I-1536-d) and 10 parts of tetrahydrofuran were mixed, stirred at 23°C for 30 minutes, cooled to 5°C, and 0.14 parts of sodium hydride was added. To the obtained mixture, 2.32 parts of a salt represented by the formula (I-236-c) was added, and after stirring at 5°C for 3 hours, the temperature was raised to 23°C and stirred at 23°C for 1 hour. To the obtained mixture, 30 parts of chloroform and 15 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. After concentrating the obtained organic layer, 1 part of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, and the formula (I-1536-f ) of the salt represented by 1.36 parts.

0.65 parts of the salt represented by the formula (I-1536-f), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The resulting organic layer was concentrated, and 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23°C for 30 minutes, and then filtered to obtain 0.76 parts of a salt represented by the formula (I-1536).

MASS(ESI(+) Spectrum):M ⁺ 782.9

MASS(ESI(-) Spectrum):M ^- 467.1

[0263] Example 14: Synthesis of the salt represented by the formula (I-1612)

2.26 parts of the compound represented by the formula (I-1536-d) and 10 parts of tetrahydrofuran were mixed, stirred at 23°C for 30 minutes, cooled to 5°C, and 0.14 parts of sodium hydride was added. To the resulting mixture, 2.32 parts of a salt represented by the formula (I-236-c) was added, and stirred at 5° C. for 3 hours. To the obtained mixture, after adding 6.30 parts of 1N hydrochloric acid, the temperature was raised to 23° C. and stirred at 23° C. for 6 hours. To the obtained mixture, 30 parts of chloroform and 15 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. After concentrating the obtained organic layer, 1 part of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant solution was removed and concentrated, and the formula (I-1612-f ) of the salt represented by 1.01 parts.

0.59 parts of the salt represented by the formula (I-1612-f), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23°C for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, and 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23 degreeC for 30 minutes, and filtered, 0.58 part of salt represented by Formula (I-1612) was obtained.

MASS(ESI(+) Spectrum):M ⁺ 710.9

MASS(ESI(-) Spectrum):M ^- 467.1

[0264] Example 15: Synthesis of salt represented by formula (I-1688)

1.00 parts of the salt represented by the formula (I-1612-f) and 30 parts of dimethylformamide are mixed, stirred at 23°C for 30 minutes, 0.08 parts of potassium carbonate and 0.03 parts of potassium iodide are added, and the temperature is raised to 75°C did it To the obtained mixture, 0.55 parts of a compound represented by the formula (I-953-a) was added, stirred at 75°C for 5 hours, and then cooled to 23°C. To the obtained mixture, 50 parts of chloroform and 20 parts of a 5% aqueous oxalic acid solution were added, stirred at 23° C. for 30 minutes, and the mixture was separated and the organic layer was extracted. 20 parts of ion-exchanged water was added to the obtained organic layer, and after stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 5 times. By concentrating the obtained organic layer, 1.11 parts of a compound represented by the formula (I-1688-b) was obtained.

0.76 parts of the salt represented by the formula (I-1688-b), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23°C for 30 minutes, and then filtered to obtain 0.94 parts of a salt represented by the formula (I-1688).

MASS(ESI(+) Spectrum):M ⁺ 917.0

MASS(ESI(-) Spectrum):M ^- 467.1

[0265] Example 16: Synthesis of the salt represented by the formula (I-1878)

2.26 parts of the compound represented by the formula (I-1536-d), 0.78 parts of the salt represented by the formula (I-915-e) and 30 parts of dimethylformamide are mixed, stirred at 23° C. for 30 minutes, and then heated to 90° C. The temperature was raised. To the resulting mixture, 1.44 parts of potassium carbonate was added, stirred at 90°C for 3 hours, and then cooled to 23°C. To the obtained mixture, 50 parts of chloroform and 30 parts of ion-exchanged water were added, and after stirring at 23°C for 30 minutes, the mixture was separated and the organic layer was extracted. 30 parts of ion-exchanged water was added to the obtained organic layer, and after stirring at 23 degreeC for 30 minute(s), it liquid-separated and the organic layer was extracted. This washing operation was repeated 3 times. After concentrating the obtained organic layer, 3 parts of acetonitrile and 30 parts of tert-butylmethyl ether were added to the concentration residue, stirred at 23° C. for 30 minutes, the supernatant was removed and concentrated, and the formula (I-1878-f ) of the salt represented by 1.91 parts.

0.94 parts of the salt represented by the formula (I-1878-f), 0.45 parts of the salt represented by the formula (I-966-g), 30 parts of chloroform and 15 parts of ethyl acetate were mixed, and stirred at 23° C. for 2 hours. To the obtained mixture, 20 parts of ion-exchanged water was added and stirred at 23°C for 30 minutes, followed by liquid separation to extract the organic layer. This washing operation was repeated 5 times. The obtained organic layer was concentrated, 30 parts of tert-butylmethyl ether was added to the concentration residue, stirred at 23°C for 30 minutes, and then filtered to obtain 1.13 parts of a salt represented by the formula (I-1878).

MASS(ESI(+) Spectrum):M ⁺ 1144.7

MASS(ESI(-) Spectrum):M ^- 467.1

[0266] Synthesis of resin

The compound (monomer) used for the synthesis|combination of resin (A) is shown below. Hereinafter, these compounds are called "monomer (a1-1-3)" etc. according to the formula number.

[0267] Synthesis Example 1 [Synthesis of Resin A1]

As a monomer, using a monomer (a1-4-2), a monomer (a1-1-3) and a monomer (a1-2-6), the molar ratio [monomer (a1-4-2):monomer (a1-1) -3):monomer (a1-2-6)] is mixed in a ratio of 38:24:38, and further, in this monomer mixture, 1.5 mass times the total mass of all monomers. Methyl isobutyl ketone was mixed. To the obtained mixture, azobisisobutyronitrile as an initiator was added so as to be 7 mol% based on the total number of moles of all monomers, and polymerization was performed by heating it at 85°C for about 5 hours. Thereafter, an aqueous solution of p-toluenesulfonic acid (2.5 wt%) in an amount of 2.0 mass times based on the total mass of all monomers was added to the polymerization reaction solution, stirred for 6 hours, and then liquid-separated. The obtained organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and collection to obtain Resin A1 (copolymer) having a ^{weight average molecular weight of about 5.3×10 3 in a yield of 78%.} This resin A1 has the following structural units.

[0268] Synthesis Example 2 [Synthesis of Resin A2]

Using the monomer (a1-4-2) and the monomer (a1-2-6) as the monomer, the molar ratio [monomer (a1-4-2):monomer (a1-2-6)] is 38:62 It mixed so that it might become the ratio of , and 1.5 mass times of methyl isobutyl ketone was mixed with this monomer mixture with respect to the total mass of all the monomers further. To the obtained mixture, azobisisobutyronitrile as an initiator was added so as to be 7 mol% based on the total number of moles of all monomers, and polymerization was performed by heating it at 85°C for about 5 hours. Thereafter, an aqueous solution of p-toluenesulfonic acid (2.5 wt%) in an amount of 2.0 mass times based on the total mass of all monomers was added to the polymerization reaction solution, stirred for 6 hours, and then liquid-separated. The obtained organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and collection to obtain Resin A2 (copolymer) having a ^{weight average molecular weight of about 5.4×10 3 in a yield of 89%.} This resin A2 has the following structural units.

[0269] Synthesis Example 3 [Synthesis of Resin A3]

As a monomer, using a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer (aa1-4-2) , the molar ratio [monomer (a1-1-3):monomer (a1-2-6):monomer (a2-1-3):monomer (a3-4-2):monomer (a1-4-2)] is , 20:35:3:15:27, and further, 1.5 mass times of methyl isobutyl ketone was mixed with this monomer mixture with respect to the total mass of all monomers. To the obtained mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis(2,4-dimethylvaleronitrile) as initiators were added, respectively, based on the total amount of monomers, and these were added at 73°C for about 5 hours. heated while Thereafter, an aqueous solution of p-toluenesulfonic acid (2.5 wt%) in an amount of 2.0 mass times based on the total mass of all monomers was added to the polymerization reaction solution, followed by stirring for 12 hours, followed by liquid separation. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery ^{to obtain Resin A3 having a weight average molecular weight of about 5.3×10 3} in a yield of 63%. This resin A3 has the following structural units.

[0270] Synthesis Example 4 [Synthesis of Resin A4]

As a monomer, using a monomer (a1-1-3), a monomer (a1-2-6), a monomer (a2-1-3), a monomer (a3-4-2) and a monomer (a1-4-13) , the molar ratio [monomer (a1-1-3):monomer (a1-2-6):monomer (a2-1-3):monomer (a3-4-2):monomer (a1-4-13)] is , 20:35:3:15:27, and further, 1.5 mass times of methyl isobutyl ketone was mixed with this monomer mixture with respect to the total mass of all monomers. To the obtained mixture, 1.2 mol% and 3.6 mol% of azobisisobutyronitrile and azobis(2,4-dimethylvaleronitrile) as initiators were added, respectively, based on the total amount of monomers, and these were added at 73°C for about 5 hours. heated while Thereafter, an aqueous solution of p-toluenesulfonic acid (2.5 wt%) in an amount of 2.0 mass times based on the total mass of all monomers was added to the polymerization reaction solution, followed by stirring for 12 hours, followed by liquid separation. The recovered organic layer was poured into a large amount of n-heptane to precipitate a resin, followed by filtration and recovery ^{to obtain Resin A4 having a weight average molecular weight of about 5.1×10 3} in a yield of 61%. This resin A4 has the following structural units.

[0271] <Preparation of resist composition>

As shown in Table 2, each of the following components was mixed, and the resulting mixture was filtered through a fluororesin filter having a pore diameter of 0.2 µm to prepare a resist composition.

[Table 2]

[0272] <Resin>

A1 to A4: Resin A1 to Resin A4

<Salt (I)>

I-236: salt represented by formula (I-236)

I-274: salt represented by formula (I-274)

I-282: salt represented by formula (I-282)

I-915: salt represented by formula (I-915)

I-920: salt represented by formula (I-920)

I-953: salt represented by formula (I-953)

I-958: salt represented by formula (I-958)

I-966: salt represented by formula (I-966)

I-1460: salt represented by formula (I-1460)

I-1536: salt represented by formula (I-1536)

I-1574: salt represented by formula (I-1574)

I-1612: salt represented by formula (I-1612)

I-1688: salt represented by formula (I-1688)

I-1764: salt represented by formula (I-1764)

I-1802: salt represented by formula (I-1802)

I-1878: salt represented by formula (I-1878)

<Acid generator>

IX-1

IX-2

IX-3

IX-4

IX-5

＜??wife (C)＞

C1: synthesized by the method described in Japanese Patent Application Laid-Open No. 2011-39502

<solvent>

Propylene glycol monomethyl ether acetate 400 copies

Propylene glycol monomethyl ether 100 copies

γ-butyrolactone Part 5

[0273] (Evaluation of resist composition by electron beam exposure: alkali development)

A 6-inch silicon wafer was treated on a direct hotplate at 90° C. for 60 seconds using hexamethyldisilazane. On this silicon wafer, the resist composition was spin-coated so that the film thickness of a composition layer might be set to 0.04 micrometer. Then, on a direct hotplate, it prebaked for 60 second at the temperature shown in the "PB" column of Table 2, and formed the composition layer. On the composition layer formed on the wafer, a contact hole pattern (hole pitch 40 nm/hole diameter 17 nm) was directly drawn by using an electron beam writer ["ELS-F125 125 keV" manufactured by ELIONIX INC.] while changing the exposure amount stepwise. did.

After exposure, PEB (post exposure bake) is performed for 60 seconds at the temperature shown in the "PEB" column of Table 2 on a hot plate, and further subjected to puddle development for 60 seconds with 2.38 mass % tetramethylammonium hydroxide aqueous solution, A resist pattern was obtained.

[0274] In the resist pattern obtained after development, the exposure amount at which the formed hole diameter became 17 nm was defined as the effective sensitivity.

[0275] <CD uniformity (CDU) evaluation>

In the effective sensitivity, the hole diameter of the pattern formed with the hole diameter of 17 nm was measured 24 times per hole, and the average value was set as the average hole diameter of one hole. The standard deviation was calculated|required using the thing which measured 400 average hole diameters of the pattern formed with the hole diameter of 17 nm in the same wafer as a population.

The results are shown in Table 3. Numerical values in the table represent standard deviations (nm).

[Table 3]

Compared with Comparative Compositions 1 to 5, the standard deviation in Compositions 1 to 20 was small, and CDU uniformity (CDU) evaluation was good.

[0276] (electron beam exposure evaluation of resist composition: organic solvent development)

A 6-inch silicon wafer was treated on a direct hotplate at 90° C. for 60 seconds using hexamethyldisilazane. On this silicon wafer, the resist composition was spin-coated so that the film thickness of a composition layer might be set to 0.04 micrometer. Then, on a direct hotplate, it prebaked for 60 second at the temperature shown in the "PB" column of Table 2, and formed the composition layer. On the composition layer formed on the wafer, a contact hole pattern (hole pitch 40 nm/hole diameter 17 nm) was directly drawn by using an electron beam writer ["ELS-F125 125 keV" manufactured by ELIONIX INC.] while changing the exposure amount stepwise. did.

After exposure, PEB (post exposure bake) was performed for 60 second at the temperature shown in the "PEB" column of Table 2 on a hotplate. Next, a resist pattern was obtained by developing the composition layer on this silicon wafer by the dynamic dispensing method at 23 degreeC for 20 second using butyl acetate (made by Tokyo Chemical Industry Co., Ltd.) as a developing solution.

[0277] In the resist pattern obtained after development, the exposure amount at which the formed hole diameter became 17 nm was defined as the effective sensitivity.

[0278] <CD uniformity (CDU) evaluation>

In the effective sensitivity, the hole diameter of the pattern formed with the hole diameter of 17 nm was measured 24 times per hole, and the average value was set as the average hole diameter of one hole. The standard deviation was calculated|required using what measured 400 average hole diameters of the pattern formed with the hole diameter of 17 nm in the same wafer as a population.

The results are shown in Table 4. Numerical values in the table represent standard deviations (nm).

[Table 4]

Compared with Comparative Compositions 6 to 10, the standard deviation in Compositions 21 to 37 was small, and CDU uniformity (CDU) evaluation was good.

[Industrial Applicability]

[0279] The resist composition containing the salt of the present invention can obtain a resist pattern having good CD uniformity (CDU), so it is suitable for microfabrication of semiconductors and is very useful in industry.

Claims (14)

A salt represented by formula (I).

[In formula (I),
R ¹ and R ² each independently represent a hydroxyl group, -OR ¹⁰ , -O-CO-OR ¹⁰ , or -OL ¹ -CO-OR ¹⁰ .
L ¹ represents an alkanediyl group having 1 to 6 carbon atoms.
R ⁴ , R ⁵ , R ⁷ and R ⁸ each independently represent a halogen atom, a fluorinated alkyl group having 1 to 12 carbon atoms or a hydrocarbon group having 1 to 18 carbon atoms, the hydrocarbon group may have a substituent, and the hydrocarbon group -CH ₂ - contained may be substituted with -O-, -CO-, -S-, or -SO _{2 -.}
R ¹⁰ represents an acid labile group.
X ¹ and X ² each independently represent an oxygen atom or a sulfur atom.
m1 represents the integer in any one of 1-5, and when m1 is 2 or more, the group in some parenthesis may mutually be same or different.
m2 represents the integer in any one of 0-5, and when m2 is 2 or more, the group in several parenthesis may mutually be same or different.
m4 represents the integer in any one of 0-4, and when m4 is 2 or more, some R<^4> may mutually be same or different.
m5 represents the integer in any one of 0-4, and when m5 is 2 or more, some R<^5> may mutually be same or different.
m7 represents the integer in any one of 0-4, and when m7 is 2 or more, some R<^7> may mutually be same or different.
m8 represents the integer in any one of 0-5, and when m8 is 2 or more, some R<^8> may mutually be same or different.
However, 1≤m1+m7≤5 and 0≤m2+m8≤5.
AI ^- represents an organic anion.] According to claim 1,
A ^{salt wherein X 1} and X ² are oxygen atoms. 3. The method of claim 1 or 2,
A ^{salt in which the acid labile group of R 10} is a group represented by the formula (1a) or a group represented by the formula (2a).

Equation (1a) of, R ^aa1, R ^aa2 and R ^aa3 is, may each independently have an alkyl group having 1 to 8 carbon atoms which may have a substituent, an alkenyl group having a carbon number of 2-8 that may have a substituent the substituents represents an alicyclic hydrocarbon group having 3 to 20 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms which may have a substituent, or R ^aa1 and R ^aa2 are bonded to each other and together with the carbon atom to which they are bonded, have 3 to 20 carbon atoms Forms an alicyclic hydrocarbon group.
* indicates a bonding hand.]

[In formula (2a), R ^aa1' and R ^aa2' each independently represent a hydrogen atom or a hydrocarbon group having 1 to 12 carbon atoms, and R ^aa3' represents a hydrocarbon group having 1 to 20 carbon atoms, or R ^{aa2 '} and R ^aa3' combine with each other to form a heterocyclic group having 3 to 20 carbon atoms together with ^{-CX a} - to which they are bonded _{, and -CH 2} - included in the hydrocarbon group and the heterocyclic group is -O- or - It may be substituted with S-.
X ^a represents an oxygen atom or a sulfur atom.
* indicates a bonding hand.] 4. The method according to any one of claims 1 to 3,
R ¹ and R ² each independently represent a hydroxy group, OR ¹⁰ , or -OL ¹ -CO-OR ¹⁰ salt. 5. The method according to any one of claims 1 to 4,
m2 is 0,
m8 is 1, and R ⁸ is an alkyl group of carbon number 3 or 4 of the basin-like, salts. 6. The method according to any one of claims 1 to 5,
A salt in which the bonding position of R ¹ is bonded at the p position with respect to the bonding position of ^{X 1 .} 7. The method according to any one of claims 1 to 6,
AI ^{- a} salt in which valence is a sulfonic acid anion, a sulfonylimide anion, a sulfonylmethide anion or a carboxylic acid anion. 8. The method according to any one of claims 1 to 7,
AI ⁻ is a sulfonic acid anion, and the sulfonic acid anion is a salt represented by the formula (IA).

[In formula (IA),
Q ¹ and Q ² each independently represent a fluorine atom or a perfluoroalkyl group having 1 to 6 carbon atoms.
L ¹ represents a saturated hydrocarbon group having 1 to 24 carbon atoms, -CH ₂ - contained in the saturated hydrocarbon group may be substituted with -O- or -CO-, and a hydrogen atom contained in the saturated hydrocarbon group is fluorine It may be substituted with an atom or a hydroxyl group.
Y ¹ represents a methyl group which may have a substituent or an alicyclic hydrocarbon group having 3 to 24 carbon atoms which may have a substituent, and -CH ₂ - contained in the alicyclic hydrocarbon group is -O-, -SO ₂ - or - It may be substituted with CO-.] An acid generator comprising the salt according to any one of claims 1 to 8. A resist composition comprising the acid generator according to claim 9 and a resin having an acid labile group. 11. The method of claim 10,
A resist composition, wherein the resin having an acid-labile group comprises at least one selected from the group consisting of a structural unit represented by formula (a1-1) and a structural unit represented by formula (a1-2).

[In formulas (a1-1) and (a1-2),
L ^a1 and L ^a2 each independently represent -O- or *-O-(CH ₂ ) _k1 -CO-O-, k1 represents an integer of any one of 1 to 7, and * is -CO- represents a bond with
R ^a4 and R ^a5 each independently represent a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^a6 and R ^a7 each independently represent an alkyl group having 1 to 8 carbon atoms, an alkenyl group having 2 to 8 carbon atoms, an alicyclic hydrocarbon group having 3 to 18 carbon atoms, an aromatic hydrocarbon group having 6 to 18 carbon atoms, or a group combining them. .
m1 represents the integer in any one of 0-14.
n1 represents the integer in any one of 0-10.
n1' represents the integer in any one of 0-3.] 12. The method of claim 10 or 11,
A resist composition wherein the resin having an acid labile group includes a structural unit represented by formula (a2-A).

[In formula (a2-A),
R ^a50 represents a hydrogen atom, a halogen atom, or an alkyl group having 1 to 6 carbon atoms which may have a halogen atom.
R ^a51 is a halogen atom, a hydroxy group, an alkyl group having 1 to 6 carbon atoms, an alkoxy group having 1 to 6 carbon atoms, an alkoxyalkyl group having 2 to 12 carbon atoms, an alkoxyalkoxy group having 2 to 12 carbon atoms, an alkylcarbonyl group having 2 to 4 carbon atoms, and an alkylcarbonyl group having 2 to 4 carbon atoms. An alkylcarbonyloxy group, acryloyloxy group or methacryloyloxy group which is 2-4 is represented.
A ^a50 represents a single bond or ^* -X ^a51 -(A ^a52 -X ^a52 ) _nb -, and * represents a bond with the carbon atom to which ^{-R a50 is bonded.}
A ^a52 represents a C1-C6 alkanediyl group.
X ^a51 and X ^a52 each independently represent -O-, -CO-O- or -O-CO-.
nb represents 0 or 1.
mb represents any integer from 0 to 4. When mb is any integer of 2 or more, a plurality of R ^a51 may be the same or different from each other.] 13. The method according to any one of claims 10 to 12,
A resist composition further comprising a salt that generates an acid having a weaker acidity than the acid generated from the acid generator. (1) a step of applying the resist composition according to any one of items 10 to 13 on a substrate;
(2) drying the composition after application to form a composition layer;
(3) a step of exposing the composition layer;
(4) heating the composition layer after exposure, and
(5) Process of developing the composition layer after heating
A method of manufacturing a resist pattern comprising a.